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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1742441생성일: 2026년 10월 26일

Progesterone → 4-(Aminomethyl)-2,6-dimethoxyphenol

https://huagongshe.com/reaction/1742441

반응식

참여 물질

역할이름HCID투입량
반응물ProgesteroneHCID 5994—
반응물4-MethylmorpholineHCID 7972—
반응물Isobutyl chloroformateHCID 62365—
반응물HCID 10154321HCID 10154321—
용매Dimethyl SulfoxideHCID 679—
용매DimethylformamideHCID 6228—
용매Carbontetrachloride dry-iceHCID 86602444—
생성물4-(Aminomethyl)-2,6-dimethoxyphenolHCID 1378048730%

반응 단계

Progesterone hemisuccinate (90 mg, 0.209 mmole) and N-methylmorpholine (22 μl, 209 mmole) were dissolved in anhydrous DMF (2 ml). The solution was chilled in dry ice/CCl4 bath and isobutylchloroformate (30 μl, 0.229 mmole) was added. After 2 minutes a solution of the acridinium (42) (101 mg, 0.143 mmole) in dimethylsulfoxide (2 ml) containing N-methylmorpholine (3.14 μl, 0.28 mmole) was added. Stirring was continued at -20° C. for 10 minutes and the cooling bath was removed. After stirring at room temperature for 7 hours, 3 drops of water were added. The solvents were removed in vacuo and ethyl acetate was added to the residue. The oily precipitate was washed repeatedly with ethyl acetate. Upon trituration with acetonitrile (2 ml) the oil separated as solids. The product was purified on HPLC using C18Dynamax semi-prep column (10 mm×250 mm) (commercially available from Rainin Instrument Co., Inc., Woburn, Mass.) using CH3CN/H2O (0.1% trifluoroacetic acid), 55/45 as mobile phase at a flow rate of 2.75 ml/min. The peak appearing at retention time of 6.00 minutes was collected. Evaporation of solvents gave the conjugate (43) (yield=30%). MS: FAB, thioglycerol matrix, 895 (M+, without any counterions).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05338847
출처 데이터셋uspto-grants-1994_08
ORD IDord-a236bfe46fb244ccb8e9b577defdced8
출처 메모uspto-grants-1994_08