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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1481028생성일: 2026년 10월 26일

(3R)-3-amino-3-phenylpropanoic acid → (R)-3-[(1-Cyano-4-hydroxy-7-phenoxy-isoquinoline-3-carbonyl)-amino]-3-phenyl-propionic acid

https://huagongshe.com/reaction/1481028

반응식

참여 물질

역할이름HCID투입량
반응물(3R)-3-amino-3-phenylpropanoic acidHCID 686703—
반응물Sodium MethoxideHCID 10942334—
반응물Methyl 1-cyano-4-hydroxy-7-phenoxyisoquinoline-3-carboxylateHCID 89812860—
용매2-MethoxyethanolHCID 8019—
생성물(R)-3-[(1-Cyano-4-hydroxy-7-phenoxy-isoquinoline-3-carbonyl)-amino]-3-phenyl-propionic acidHCID 71737525—

반응 단계

Methyl 1-cyano-4-hydroxy-7-phenoxyisoquinoline-3-carboxylate (20 mg, 0.06 mmol), (R)-3-amino-3-phenyl-propionic acid (62 mg, 0.38 mmol, PepTech) and sodium methoxide (19 mg, 0.35 mmol) were suspended in 2-methoxyethanol (3 mL). The resulting mixture was heated to reflux for 3 hours and then cooled to room temperature. The solvent was removed in vacuo and the residue was dissolved in H2O (15 mL) and EtOAc (15 mL). To the stirred mixture was added 1 N hydrochloric acid until pH was 1. The layers were separated and the aqueous layer was extracted twice with EtOAc. The combined organic layers were dried over MgSO4, concentrated, and purified by flash chromatography (0-50% EtOAc/CH2Cl2 with 0.5% formic acid) to give the title compound in 17 mg. MS: (−) m/z 451.93 (M−1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09409892B2
출처 데이터셋uspto-grants-2016_08
ORD IDord-11613c29fc154c42b7661b7bd0258354
출처 메모uspto-grants-2016_08