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HRID 84967作成日:2026年10月23日

Benzenesulfonyl chloride, 3,4-dichloro- → tert-Butyl trans-6-[(3,4-dichlorophenyl)sulfonyl]-6,7,7a,8,10,10a-hexahydropyrido[3,2-c]pyrrolo[3,4-e]azepine-9(5H)-carboxylate

https://huagongshe.com/ja/reaction/84967

反応式

関与物質

役割名称HCID仕込み量
反応物Benzenesulfonyl chloride, 3,4-dichloro-HCID 7383—
反応物TriethylamineHCID 8471—
反応物Sodium HydroxideHCID 14798—
反応物tert-Butyl trans-6,7,7a,8,10,10a-hexahydropyrido[3,2-c]pyrrolo[3,4-e]azepine-9(5H)-carboxylateHCID 123947677—
溶媒DichloromethaneHCID 6344—
生成物tert-Butyl trans-6-[(3,4-dichlorophenyl)sulfonyl]-6,7,7a,8,10,10a-hexahydropyrido[3,2-c]pyrrolo[3,4-e]azepine-9(5H)-carboxylateHCID 123445055—

反応手順

A mixture of Example 334B (100 mg, 0.34 mmol) and triethylamine (0.097 mL, 0.69 mmol) in dichloromethane (2 mL) was stirred at ambient temperature for 10 minutes. 3,4-Dichlorobenzene-1-sulfonyl chloride (0.52 mmol, 1.5 equivalents) was added, and the reaction mixture was stirred at room temperature overnight. A 10% NaOH solution (2 mL) was added; the dichloromethane layer was separated, treated with water (2 mL) and dried over Na2SO4. The solvent was removed in vacuo to give the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846951B2
出典データセットuspto-grants-2014_09
ORD IDord-f6e17a941eae4d229020d7b4426a778f
出典メモuspto-grants-2014_09