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HRID 428858作成日:2026年10月26日

Pyridine → N-[3-(3-Hexyl-6-methyl-3-azabicyclo[3.1.0]hex-6-yl)phenyl]-2-methoxy-1-ethanesulfonamide

https://huagongshe.com/reaction/428858

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物2-Methoxyethane-1-sulfonyl chlorideHCID 13480221—
反応物3-(3-Hexyl-6-methyl-3-azabicyclo[3.1.0]hex-6-yl)phenylamineHCID 22141322—
溶媒DichloromethaneHCID 6344—
生成物N-[3-(3-Hexyl-6-methyl-3-azabicyclo[3.1.0]hex-6-yl)phenyl]-2-methoxy-1-ethanesulfonamideHCID 9822011—

反応手順

To a solution of 3-(3-hexyl-6-methyl-3-azabicyclo[3.1.0]hex-6-yl)phenylamine (Preparation 12, 0.11 g, 0.40 mmol) in dichloromethane (1.5 ml) was added pyridine (64 mg) in dichloromethane (0.75 ml) and 2-methoxy-1-ethanesulfonyl chloride (J. F. King, J. Y. L. Lam, S. Kronieczny, J. Am. Chem. Soc., 1992, 114 (5), 1743; 0.96 g, 0.60 mmol). The reaction mixture was stirred at room temperature for 16 h and then concentrated in vacuo. The crude residue was purified by chromatography on silica gel eluting with ethyl acetate: 2M ammonia in methanol (99:1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06313312B1
出典データセットuspto-grants-2001_11
ORD IDord-877775520341421197d67e2105cbe7dc
出典メモuspto-grants-2001_11