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HRID 453951作成日:2026年10月27日

Isovalerate → (2S)-3-methyl-2-[pentanoyl-[[4-[2-(2H-tetrazol-5-yl)phenyl]phenyl]methyl]amino]-5,5,5-triphenylpentanoic acid

https://huagongshe.com/reaction/453951

反応式

関与物質

役割名称HCID仕込み量
反応物IsovalerateHCID 3587356—
反応物2-(1-Trityl-1H-tetrazol-5-YL)phenylboronic acidHCID 10342745—
反応物(S)-Methyl 3-methyl-2-(N-((2'-(1-trityl-1H-tetrazol-5-yl)-[1,1'-biphenyl]-4-yl)methyl)pentanamido)butanoateHCID 16726602—
生成物(2S)-3-methyl-2-[pentanoyl-[[4-[2-(2H-tetrazol-5-yl)phenyl]phenyl]methyl]amino]-5,5,5-triphenylpentanoic acidHCID 21051452—

反応手順

WO 2007/005967 discloses the condensation of p-Bromobenzylbromide with valine methyl ester to give (S)-methyl-2-(4-bromobenzylamino)-3-methyl butanoate which on reaction with valeryl chloride to give (S)-methyl-2-(4-bromobenzyl)pentanamido)-3-methylbutanoate. (S)-methyl-2-(4-bromobenzyl)pentanamido)-3-methylbutanoate is treated with 2-(1-trityl-1H-tetrazol-5-yl)phenylboronic acid to give (S)-3-methyl-2-{pentanoyl-[2′-(1-trityl-1H-tetrazol-5-yl)biphenyl-4-ylmethyl]amino}butyric acid methyl ester and base hydrolysis to give trityl valsartan. Triltyl valsartan is treated with an acid to give valsartan.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08492577B2
出典データセットuspto-grants-2013_07
ORD IDord-632a418b51574626bf30def58d43d16d
出典メモuspto-grants-2013_07