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HRID 225433作成日:2026年10月25日

Pyridine → tert-Butyl 2-[3-chloro-4-(3-oxomorpholin-4-yl)phenylcarbamoyl]pyrazolidine-1-carboxylate

https://huagongshe.com/reaction/225433

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物DiisopropylethylamineHCID 81531—
反応物4-Nitrophenyl chloroformateHCID 82129—
反応物tert-Butyl pyrazolidine-1-carboxylateHCID 21857793—
反応物4-(4-Amino-2-chlorophenyl)morpholin-3-oneHCID 23105327—
溶媒DichloromethaneHCID 6344—
生成物tert-Butyl 2-[3-chloro-4-(3-oxomorpholin-4-yl)phenylcarbamoyl]pyrazolidine-1-carboxylateHCID 86607077—

反応手順

340 mg (1.5 mmol) of 4-(4-amino-2-chlorophenyl)morpholin-3-one are dissolved in 10 ml of dichloromethane (DCM), 302 mg (1.5 mmol) of 4-nitrophenyl chloroformate and 121 μl (1.5 mmol) of pyridine are subsequently added successively, and the mixture is stirred at RT for 1 h. 300.0 mg (0.7 mmol) of tert-butyl pyrazolidine-1-carboxylate and 0.765 mg (4.5 mmol) of N-ethyldiisopropylamine are added to this reaction mixture. After stirring at RT for 20 h, the mixture is subjected to conventional work-up, giving 420 mg (57.3%) of step 1; MS (FAB) m/e=425/427 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07557102B2
出典データセットuspto-grants-2009_07
ORD IDord-205a888a3d854f2a95982cedf6ba42b4
出典メモuspto-grants-2009_07