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HRID 1084527作成日:2026年10月25日

Dicyclohexylcarbodiimide → 1,3-Dihydro-5-(2-fluorophenyl)-3(RS)-(2-thienyl)methyl-2H-1,4-benzodiazepin-2-one

https://huagongshe.com/reaction/1084527

反応式

関与物質

役割名称HCID仕込み量
反応物DicyclohexylcarbodiimideHCID 10868—
反応物2-Amino-2'-fluorobenzophenoneHCID 74101—
反応物N-Boc-beta-(2-thienyl)-DL-alanineHCID 5035100—
溶媒DichloromethaneHCID 6344—
生成物1,3-Dihydro-5-(2-fluorophenyl)-3(RS)-(2-thienyl)methyl-2H-1,4-benzodiazepin-2-oneHCID 15614738—

反応手順

The procedure of Example 1 was carried out using 2-amino-2'-fluorobenzophenone (1.26 gm, 5.86 mmol), N-Boc-β-(2-thienyl)-DL-alanine (1.75 gm, 6.45 mmol), and DCC (6.45 ml of 1.0M solution in CH2Cl2) in CH2Cl2 (25 ml). Filtration, concentration in vacuo and flash chromatography (silica gel, 1% (v/v) Et2O in CH2Cl2) gave a white foam which was deprotected and cyclized by the procedure of Example 2. After stirring 3 days, the mixture was evaporated in vacuo, treated with H2O (50 ml) and extracted with EtOAc (2×100 ml). The combined organic extracts were washed with brine (50 ml), dried over MgSO4, filtered, and evaporated to dryness in vacuo. The resulting foam was crystallized from Et2O to give the title compound as a white solid. The solid was dried in vacuo at 65° C.: (m.p. 189°-91° C.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05004741
出典データセットuspto-grants-1991_04
ORD IDord-be44ebf39bb64895b9c5643b3f3e7122
出典メモuspto-grants-1991_04