Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2065928생성일: 2026년 10월 27일
Benzyl Alcohol → 1H-Indole-2-carboxylic acid, octahydro-, phenylmethyl ester, hydrochloride (1:1), (2S,3aR,7aS)-
https://huagongshe.com/reaction/2065928
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Benzyl Alcohol | HCID 244 | — |
| 반응물 | Thionyl Chloride | HCID 24386 | — |
| 반응물 | (2S,3aR,7aS)-octahydro-1H-indole-2-carboxylic acid | HCID 7018901 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 1H-Indole-2-carboxylic acid, octahydro-, phenylmethyl ester, hydrochloride (1:1), (2S,3aR,7aS)- | HCID 11645051 | — |
반응 단계
Additionally, as depicted in FIG. 3, the production of (2S,3aR,7aS)-benzyl octahydro-1H-indole-2-carboxylate hydrochloride salt (3), a key intermediate in the production of trandolaprilat and trandolapril, may be produced using a starting material of crystalline ((1S,2S)-2-((S)-1-phenylethylamino)cyclohexyl)methanol (11). The first step of the process involves reaction with a catalyst including, but not limited to, palladium on carbon or palladium hydroxide on carbon in the presence of an alcohol such as methanol to produce ((1S,2S)-2-aminocyclohexyl)methanol (17). The remaining steps in the conversion of compound (17) to the hydrochloride salt, and eventual conversion to (2S,3aR,7aS)-benzyl octahydro-1H-indole-2-carboxylate hydrochloride salt (3) are based upon the teachings of U.S. Pat. No. 4,879,392, which is fully incorporated herein by reference. Generally, the remaining steps can be described as follows. Compound (17) is subjected to treatment with sodium cyanide in the presence of formaldehyde to produce compound (18), as illustrated in FIG. 3. Subsequently, compound (18) is first reacted with trimethylsilyl chloride, and then the product of that reaction is treated with benzyl chloride to produce compound (19). Further, compound (19) is then subjected to three sequential reactions to produce compound (20) as illustrated in FIG. 3. Specifically, compound (19) is first subjected to treatment with hydrochloric acid. Subsequently, methanesulfonyl chloride is added to the reaction mixture. Thereafter, potassium hydroxide is added to the reaction to produce compound (20). After compound (20) is produced, the compound is treated with aqueous mineral acid to produce the hydrochloride salt of compound (5), as disclosed previously. As described previously, compound (5) may then be treated with thionyl chloride, benzyl alcohol, and dichloromethane to produce (2S,3aR,7aS)-benzyl octahydro-1H-indole-2-carboxylate hydrochloride salt (3).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08288565B2 |
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| 출처 데이터셋 | uspto-grants-2012_10 |
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| ORD ID | ord-83a78b0e93ef45929c402cb91b28f1bb |
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| 출처 메모 | uspto-grants-2012_10 |
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