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HRID 1009812作成日:2026年10月27日

Pyridine → N-[1-(S)-Ethoxycarbonyl-3-phenylpropyl]-L-alanine-N-carboxyanhydride

https://huagongshe.com/reaction/1009812

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物TriphosgeneHCID 94429—
反応物N-[1(S)-Ethoxycarbonyl-3-phenylpropyl]-L-alanineHCID 5702571—
反応物Disodium dihydrogen phosphate dihydrateHCID 131728993—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物N-[1-(S)-Ethoxycarbonyl-3-phenylpropyl]-L-alanine-N-carboxyanhydrideHCID 4639425—

反応手順

Disodium dihydrogen phosphate dihydrate (177 gms; 0.994 moles) was dissolved in water (300 ml) at 35° C. and cooled to ambient temperature. Dichloromethane (250 ml) was charged and stirred for 15 mins. N-[1-(S)-ethoxy carbonyl-3-phenyl propyl]-L-alanine (106 gms; 0.381 moles) was added to the above solution and the reaction mass was cooled to 15° C. Solution of triphosgene (52.8 gms; 0.177 moles) dissolved dichloromethane (40 ml) was added dropwise to the reaction mass in 40 mins at 15-20° C. The reaction mass was further stirred for 30 min. Pyridine (0.5 ml; 0.006 moles) was added and the reaction mass was stirred for 1 hr at 15-20° C. The reaction mass was settled and layers were separated. Organic layer was washed with 2N HCl till the neutral pH obtained. The organic layer was further washed with water and dried over sodium sulphate. The solvent was evaporated to residue (110 gms).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07973173B2
出典データセットuspto-grants-2011_07
ORD IDord-f600f994792b486984d622730424ab60
出典メモuspto-grants-2011_07