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HRID 1084548作成日:2026年10月25日

4-Propylbenzoyl chloride → N-(2-Oxo-5-phenyl-2,3-dihydro-1H-benzo[e][1,4]diazepin-3-yl)-4-propyl-benzamide

https://huagongshe.com/reaction/1084548

反応式

関与物質

役割名称HCID仕込み量
反応物4-Propylbenzoyl chlorideHCID 104293—
反応物3-Amino-5-phenyl-1,3-dihydro-1,4-benzodiazepin-2-oneHCID 4259649—
生成物N-(2-Oxo-5-phenyl-2,3-dihydro-1H-benzo[e][1,4]diazepin-3-yl)-4-propyl-benzamideHCID 14208261—

反応手順

The procedure of Example 134 was carried out using 3(RS)-amino-1,3-dihydro-5-phenyl-2H-1,4-benzodiazepin-2-one (39.2 mg, 0.156 mmole) in place of 1,3-dihydro-3(RS)-amino-5-(2-fluorophenyl)-2H-1,4-benzodiazepin-2-one and 4-n-propylbenzoyl chloride (28.5 mg, 0.156 mmole) in place of p-trifluoromethylbenzoyl chloride. The product was chromatographed on silica gel (15% (v/v) Et2O in CH2Cl2 elution). The combined product fractions were evaporated to dryness in vacuo and crystallized from Et2O to give the title compound which was dried in vacuo at 82° C.: (m.p.. 158°-162° 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-ad457ee4899c4219b80559ca376e420e
出典メモuspto-grants-1991_04