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HRID 1742441作成日:2026年10月27日

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

https://huagongshe.com/reaction/1742441

反応式

関与物質

役割名称HCID仕込み量
反応物ProgesteroneHCID 5994—
反応物4-MethylmorpholineHCID 7972—
反応物Isobutyl chloroformateHCID 62365—
反応物AcridiniumHCID 10154321—
溶媒Dimethyl SulfoxideHCID 679—
溶媒DimethylformamideHCID 6228—
溶媒Carbontetrachloride dry-iceHCID 86602444—
生成物4-(Aminomethyl)-2,6-dimethoxyphenolHCID 1378048730%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05338847
出典データセットuspto-grants-1994_08
ORD IDord-a236bfe46fb244ccb8e9b577defdced8
出典メモuspto-grants-1994_08