Loading…
A High Yield and Pilot-Scale Process for the Preparation of Adapalene
Strategies that were adopted during the process development of adapalene to achieve a cost-effective commercial-scale synthesis are described herein. These included (1) the use of AcOH/H2SO4 to afford 2-(1-adamantyl)-4-bromophenol in quantitative yield; (2) the dimethyl sulfate methylation to enhanc...
Saved in:
Published in: | Organic process research & development 2006-03, Vol.10 (2), p.285-288 |
---|---|
Main Authors: | , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-a325t-d858cb499341fcd57027dfd2af475d9b8072673184c04b1fad0b24c086b56fcf3 |
---|---|
cites | cdi_FETCH-LOGICAL-a325t-d858cb499341fcd57027dfd2af475d9b8072673184c04b1fad0b24c086b56fcf3 |
container_end_page | 288 |
container_issue | 2 |
container_start_page | 285 |
container_title | Organic process research & development |
container_volume | 10 |
creator | Liu, Zhichang Xiang, Jiannan |
description | Strategies that were adopted during the process development of adapalene to achieve a cost-effective commercial-scale synthesis are described herein. These included (1) the use of AcOH/H2SO4 to afford 2-(1-adamantyl)-4-bromophenol in quantitative yield; (2) the dimethyl sulfate methylation to enhance the yield of methylation to 95%; (3) direct conversion of the Grignard reagent into methyl 6-(3-(1-adamantyl)-4-methoxyphenyl)-2-naphthoate by the catalysis of both PdCl2(PPh3)2 and ZnCl2 in high yield; (4) the use of EDTA-disodium salt dihydrate to ensure the heavy metal's content within acceptable limits; (5) the use of toluene to simplify the original chromatographic purification to recrystallization. The pilot-scale synthesis of adapalene is described in detail in the Experimental Section. |
doi_str_mv | 10.1021/op050223f |
format | article |
fullrecord | <record><control><sourceid>acs_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1021_op050223f</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>c385441559</sourcerecordid><originalsourceid>FETCH-LOGICAL-a325t-d858cb499341fcd57027dfd2af475d9b8072673184c04b1fad0b24c086b56fcf3</originalsourceid><addsrcrecordid>eNptj01LAzEYhIMoWKsH_0EuHjxE3ySbbPa4lNoKBQsq6GnJp92ybpZkPfjv3VLx5Glm4GGYQeiawh0FRu_jAAIY4-EEzahgQISSb6eTB8WJpBLO0UXOewAQkrIZWtZ43X7s8HvrO4d17_C27eJInq3uPN6maH3OOMSEx90h-0EnPbaxxzHg2ulhwnp_ic6C7rK_-tU5en1YvizWZPO0elzUG6I5EyNxSihriqriBQ3WiRJY6YJjOhSlcJVRUDJZcqoKC4WhQTswbPJKGiGDDXyObo-9NsWckw_NkNpPnb4bCs3hf_P3f2Jvjqy2udnHr9RPy_7hfgBWg1hE</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>A High Yield and Pilot-Scale Process for the Preparation of Adapalene</title><source>American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list)</source><creator>Liu, Zhichang ; Xiang, Jiannan</creator><creatorcontrib>Liu, Zhichang ; Xiang, Jiannan</creatorcontrib><description>Strategies that were adopted during the process development of adapalene to achieve a cost-effective commercial-scale synthesis are described herein. These included (1) the use of AcOH/H2SO4 to afford 2-(1-adamantyl)-4-bromophenol in quantitative yield; (2) the dimethyl sulfate methylation to enhance the yield of methylation to 95%; (3) direct conversion of the Grignard reagent into methyl 6-(3-(1-adamantyl)-4-methoxyphenyl)-2-naphthoate by the catalysis of both PdCl2(PPh3)2 and ZnCl2 in high yield; (4) the use of EDTA-disodium salt dihydrate to ensure the heavy metal's content within acceptable limits; (5) the use of toluene to simplify the original chromatographic purification to recrystallization. The pilot-scale synthesis of adapalene is described in detail in the Experimental Section.</description><identifier>ISSN: 1083-6160</identifier><identifier>EISSN: 1520-586X</identifier><identifier>DOI: 10.1021/op050223f</identifier><language>eng</language><publisher>American Chemical Society</publisher><ispartof>Organic process research & development, 2006-03, Vol.10 (2), p.285-288</ispartof><rights>Copyright © 2006 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a325t-d858cb499341fcd57027dfd2af475d9b8072673184c04b1fad0b24c086b56fcf3</citedby><cites>FETCH-LOGICAL-a325t-d858cb499341fcd57027dfd2af475d9b8072673184c04b1fad0b24c086b56fcf3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27915,27916</link.rule.ids></links><search><creatorcontrib>Liu, Zhichang</creatorcontrib><creatorcontrib>Xiang, Jiannan</creatorcontrib><title>A High Yield and Pilot-Scale Process for the Preparation of Adapalene</title><title>Organic process research & development</title><addtitle>Org. Process Res. Dev</addtitle><description>Strategies that were adopted during the process development of adapalene to achieve a cost-effective commercial-scale synthesis are described herein. These included (1) the use of AcOH/H2SO4 to afford 2-(1-adamantyl)-4-bromophenol in quantitative yield; (2) the dimethyl sulfate methylation to enhance the yield of methylation to 95%; (3) direct conversion of the Grignard reagent into methyl 6-(3-(1-adamantyl)-4-methoxyphenyl)-2-naphthoate by the catalysis of both PdCl2(PPh3)2 and ZnCl2 in high yield; (4) the use of EDTA-disodium salt dihydrate to ensure the heavy metal's content within acceptable limits; (5) the use of toluene to simplify the original chromatographic purification to recrystallization. The pilot-scale synthesis of adapalene is described in detail in the Experimental Section.</description><issn>1083-6160</issn><issn>1520-586X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNptj01LAzEYhIMoWKsH_0EuHjxE3ySbbPa4lNoKBQsq6GnJp92ybpZkPfjv3VLx5Glm4GGYQeiawh0FRu_jAAIY4-EEzahgQISSb6eTB8WJpBLO0UXOewAQkrIZWtZ43X7s8HvrO4d17_C27eJInq3uPN6maH3OOMSEx90h-0EnPbaxxzHg2ulhwnp_ic6C7rK_-tU5en1YvizWZPO0elzUG6I5EyNxSihriqriBQ3WiRJY6YJjOhSlcJVRUDJZcqoKC4WhQTswbPJKGiGDDXyObo-9NsWckw_NkNpPnb4bCs3hf_P3f2Jvjqy2udnHr9RPy_7hfgBWg1hE</recordid><startdate>20060301</startdate><enddate>20060301</enddate><creator>Liu, Zhichang</creator><creator>Xiang, Jiannan</creator><general>American Chemical Society</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20060301</creationdate><title>A High Yield and Pilot-Scale Process for the Preparation of Adapalene</title><author>Liu, Zhichang ; Xiang, Jiannan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a325t-d858cb499341fcd57027dfd2af475d9b8072673184c04b1fad0b24c086b56fcf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Zhichang</creatorcontrib><creatorcontrib>Xiang, Jiannan</creatorcontrib><collection>CrossRef</collection><jtitle>Organic process research & development</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Zhichang</au><au>Xiang, Jiannan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A High Yield and Pilot-Scale Process for the Preparation of Adapalene</atitle><jtitle>Organic process research & development</jtitle><addtitle>Org. Process Res. Dev</addtitle><date>2006-03-01</date><risdate>2006</risdate><volume>10</volume><issue>2</issue><spage>285</spage><epage>288</epage><pages>285-288</pages><issn>1083-6160</issn><eissn>1520-586X</eissn><abstract>Strategies that were adopted during the process development of adapalene to achieve a cost-effective commercial-scale synthesis are described herein. These included (1) the use of AcOH/H2SO4 to afford 2-(1-adamantyl)-4-bromophenol in quantitative yield; (2) the dimethyl sulfate methylation to enhance the yield of methylation to 95%; (3) direct conversion of the Grignard reagent into methyl 6-(3-(1-adamantyl)-4-methoxyphenyl)-2-naphthoate by the catalysis of both PdCl2(PPh3)2 and ZnCl2 in high yield; (4) the use of EDTA-disodium salt dihydrate to ensure the heavy metal's content within acceptable limits; (5) the use of toluene to simplify the original chromatographic purification to recrystallization. The pilot-scale synthesis of adapalene is described in detail in the Experimental Section.</abstract><pub>American Chemical Society</pub><doi>10.1021/op050223f</doi><tpages>4</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1083-6160 |
ispartof | Organic process research & development, 2006-03, Vol.10 (2), p.285-288 |
issn | 1083-6160 1520-586X |
language | eng |
recordid | cdi_crossref_primary_10_1021_op050223f |
source | American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list) |
title | A High Yield and Pilot-Scale Process for the Preparation of Adapalene |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-15T04%3A54%3A18IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-acs_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20High%20Yield%20and%20Pilot-Scale%20Process%20for%20the%20Preparation%20of%20Adapalene&rft.jtitle=Organic%20process%20research%20&%20development&rft.au=Liu,%20Zhichang&rft.date=2006-03-01&rft.volume=10&rft.issue=2&rft.spage=285&rft.epage=288&rft.pages=285-288&rft.issn=1083-6160&rft.eissn=1520-586X&rft_id=info:doi/10.1021/op050223f&rft_dat=%3Cacs_cross%3Ec385441559%3C/acs_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-a325t-d858cb499341fcd57027dfd2af475d9b8072673184c04b1fad0b24c086b56fcf3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |