{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,12]],"date-time":"2025-10-12T18:41:21Z","timestamp":1760294481465,"version":"build-2065373602"},"reference-count":15,"publisher":"Wiley","issue":"19","license":[{"start":{"date-parts":[[2018,8,31]],"date-time":"2018-08-31T00:00:00Z","timestamp":1535673600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"DOI":"10.13039\/501100001871","name":"Funda\u00e7\u00e3o para a Ci\u00eancia e a Tecnologia","doi-asserted-by":"publisher","award":["IF\/00732\/2013","SFRH\/BD\/117931\/2016","UID\/DTP\/04138\/2013"],"award-info":[{"award-number":["IF\/00732\/2013","SFRH\/BD\/117931\/2016","UID\/DTP\/04138\/2013"]}],"id":[{"id":"10.13039\/501100001871","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["chemistry-europe.onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["ChemMedChem"],"published-print":{"date-parts":[[2018,10,8]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>A more sustainable process for the synthesis of the long\u2010acting muscarinic acetylcholine antagonist umeclidinium bromide is described. Specifically, we report the synthesis of ethyl 1\u2010(2\u2010chloroethyl)\u20104\u2010piperidinecarboxylate, a key intermediate in the preparation of umeclidinium bromide, in good yields using triethylamine, as well as the identification and characterization of the by\u2010product formed in this reaction. This new method of synthesis leads to an improvement in yield over that of previously reported protocols using potassium carbonate as base (65.6\u2009% versus 38.6\u2009%). Moreover, in the final synthetic step of the process to obtain umeclidinium bromide, we were able to replace the use of toxic solvents (acetonitrile\/chloroform) with water. The use of this green solvent allowed precipitation of the active pharmaceutical ingredient (API) from the reaction medium with high purity and in high yield. Overall, we have developed a more efficient and environmentally friendly process for the synthesis of the umeclidinium bromide API with a higher overall yield (37.8\u2009% versus previously reported overall yield of 9.7\u2009%).<\/jats:p>","DOI":"10.1002\/cmdc.201800387","type":"journal-article","created":{"date-parts":[[2018,8,4]],"date-time":"2018-08-04T18:11:56Z","timestamp":1533406316000},"page":"2053-2056","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["A More Sustainable Process for Preparation of the Muscarinic Acetylcholine Antagonist Umeclidinium Bromide"],"prefix":"10.1002","volume":"13","author":[{"given":"Margarida","family":"Espadinha","sequence":"first","affiliation":[{"name":"Research Institute for Medicines (iMed.ULisboa) Faculty of Pharmacy Universidade de Lisboa  Av. 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