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HRID 356174作成日:2026年10月25日

Chloroacetyl chloride → (3aR*,10aS*)-9-Benzyl-4-(chloroacetyl)-2,3,3a,4,9,10a-hexahydrobenzo[b]cyclopenta[e][1,4]diazepin-10(1H)-one

https://huagongshe.com/reaction/356174

反応式

関与物質

役割名称HCID仕込み量
反応物Chloroacetyl chlorideHCID 6577—
反応物(3aR*,10aS*)-9-benzyl-2,3,3a,4,9,10a-hexahydrobenzo[b]cyclopenta [e][1,4]diazepin-10(1H)-oneHCID 70109795—
溶媒1,2-DichloroethaneHCID 11—
生成物(3aR*,10aS*)-9-Benzyl-4-(chloroacetyl)-2,3,3a,4,9,10a-hexahydrobenzo[b]cyclopenta[e][1,4]diazepin-10(1H)-oneHCID 7011019288%

反応手順

On a water-bath kept at 14° C., to a solution of (3aR*,10aS*)-9-benzyl-2,3,3a,4,9,10a-hexahydrobenzo[b]cyclopenta[e][1,4]diazepin-10(1H)-one (5.85 g, 20 mmol) in 1,2-dichloroethane (20 mL) was added dropwise a solution of chloroacetyl chloride (2.5 g, 22 mmol) in 1,2-dichloroethane (15 mL), and the mixture was stirred for 10 minutes. The aqueous layer of this mixture was separated, and the organic layer was washed with water and a saturated aqueous solution of sodium chloride, dried over magnesium sulfate, which was subjected to filtration, and the filtrate was concentrated under reduced pressure. The concentrate was recrystallized from dichloromethane-hexane to give 6.49 g (yield 88%) of the titled compound, m.p. 154°-156° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05834463
出典データセットuspto-grants-1998_11
ORD IDord-ff6fcf84233f492ebcd5935e0b4a2bcf
出典メモuspto-grants-1998_11