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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 24615생성일: 2026년 10월 24일

3,3-Diphenylpropylamine → 3-Carbamoyl-4-(3-chlorophenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylic acid (3,3-diphenylpropyl)amide

https://huagongshe.com/ko/reaction/24615

반응식

참여 물질

역할이름HCID투입량
반응물3,3-DiphenylpropylamineHCID 79698—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물3-Carbamoyl-4-(3-chlorophenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylic acidHCID 22570205—
용매DimethylformamideHCID 6228—
생성물3-Carbamoyl-4-(3-chlorophenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylic acid (3,3-diphenylpropyl)amideHCID 20758914—

반응 단계

102 mg (0.329 mmol) of 3-carbamoyl-4-(3-chlorophenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylic acid and 83.5 mg (0.395 mmol) of (3,3-diphenylpropyl)amine were dissolved in 10 ml of DMF. 94.6 mg (0.494 mmol) of WSC hydrochloride was added to the obtained solution under cooling with ice, and they were stirred at room temperature overnight. After the concentration under reduced pressure, the reaction mixture was diluted with ethyl acetate and then washed with 1 N hydrochloric acid, saturated aqueous sodium hydrogencarbonate solution and saturated aqueous sodium chloride solution. The organic layer was dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residue was purified by the basic silica gel chromatography (dichloromethane/methanol=100/1 to 10/1) to obtain the crude title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06855716B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-7dec7d03f2974fa1bdcd7c1807e14982
출처 메모uspto-grants-2005_02