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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 133063생성일: 2026년 10월 25일

1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride → HCID 131726935, 화합물

https://huagongshe.com/reaction/133063

반응식

참여 물질

역할이름HCID투입량
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물(R)-3-(tert-butoxycarbonylamino)-4-(2,4,5-trifluorophenyl)butanoic acidHCID 7146288—
반응물2-(Trifluoromethyl)-5,6,7,8-tetrahydro[1,2,4]triazolo[1,5-a]pyrazineHCID 34176329—
반응물HCID 178418300HCID 178418300—
용매DimethylformamideHCID 6228—
생성물HCID 131726935HCID 131726935—

반응 조건

온도0 °C

반응 단계

To a solution of 2-(trifluoromethyl)-5,6,7,8-tetrahydro[1,2,4]triazolo[1,5-α]pyrazine (28.8 mg, 0.15 mmol, from Step D) and (3R)-3-[(tert-butoxycarbonyl)amino]-4-(2,4,5-trifluorophenyl)butanoic acid (Intermediate 3, 50.0 mg, 0.15 mmol) in DMF (3 mL) was added hydroxybenzotriazole (HOBT, 26.1 mg, 0.19 mmol) at 0° C. The reaction was stirred at 0° C. for 5 min, then 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC, 37.0 mg, 0.19 mmol) was added. After removal of the ice-bath, the reaction was allowed to stir at ambient temperature for 16 h. After removal of the DMF by evaporation, the residue was partitioned between ethyl acetate and aqueous sodium bicarbonate. The aqueous layer was extracted three times with ethyl acetate. The combined organic layers were washed with brine and dried over magnesium sulfate. Concentration followed by preparative TLC (10% methanol/dichloromethane) gave the title compound as a foamy solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07390809B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-b5e5f08436f8435b8fc276c0c2b74f5a
출처 메모uspto-grants-2008_06