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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 54050생성일: 2026년 10월 24일

p-Toluenesulfonic acid → HCID 70041042, 화합물

https://huagongshe.com/ko/reaction/54050

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물EthylmorpholineHCID 7525—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물N-carbobenzyloxyalanineHCID 736104—
반응물HCID 70041054HCID 70041054—
반응물HCID 178418300HCID 178418300—
촉매PalladiumHCID 23938—
용매IsopropanolHCID 3776—
용매Ethyl AcetateHCID 8857—
생성물HCID 70041042HCID 7004104236.8%

반응 단계

1.3 g (2.79 mmol) of N-[[N-(benzyloxycarbonyl)-L-phenylalanyl]methyl]-L-proline tert.butyl ester was hydrogenated in a mixture of 10 ml of ethyl acetate and 10 ml of isopropyl alcohol in the presence of 0.39 g of 5% palladium-on-carbon and 1.06 g (5.58 mmol) of toluene-4-sulphonic acid and the product was coupled with 0.62 g (2.78 mmol) of N-(benzyloxycarbonyl)-L-alanine in the presence of 0.572 g (2.78 mmol) of dicyclohexylcarbodiimide, 0.375 g (2.78 mmol) of hydroxybenzotriazole and 0.64 g (5.57 mmol) of N-ethylmorpholine in a manner analogous to that described in Example 1. After working-up and chromatography on silica gel using 3% isopropanol in dichloromethane for the elution there was obtained 0.55 g of N-[[N-[N-(benzyloxycarbonyl)-L-alanyl]-L-phenylalanyl]methyl]-L-proline tert.butyl ester as a solid: MS: m/e 538 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05620987
출처 데이터셋uspto-grants-1997_04
ORD IDord-bf8811fec9bd460b876244d610a99ed6
출처 메모uspto-grants-1997_04