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HRID 490416作成日:2026年10月26日

2-Methylbenzenesulfonamide → HCID 18444621、化合物

https://huagongshe.com/reaction/490416

反応式

関与物質

役割名称HCID仕込み量
反応物2-MethylbenzenesulfonamideHCID 6924—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物4-([(4'-Difluoromethoxy-biphenyl-4-yl)-methyl-amino]-methyl)-5-methyl-furan-2-carboxylic acidHCID 18444565—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒AcetonitrileHCID 6342—
溶媒DichloromethaneHCID 6344—
生成物HCID 18444621HCID 184446219.9%

反応手順

A stirred solution of 4-{[(4′-difluoromethoxy-biphenyl-4-yl)-methyl-amino]-methyl}-5-methyl-furan-2-carboxylic acid (176) (21 mg, 0.054 mmoles), 2-methyl-benzenesulphonamide (19 mg, 0.108 mmoles) and 4-(N,N-dimethylamino)-pyridine (1 mg) in a mixture of dichloromethane (8 ml) and acetonitrile (2 ml) was treated with 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (11.4 mg, 0.060 mmoles). The mixture was stirred at room temperature for 18 hours under an argon atmosphere. The reaction mixture was concentrated in vacuo and the residue was purified by HPLC to afford compound 177 (2.9 mg) as a solid. LC/MS System D; Rt=11.21 mins, m/z (ES+)=541 (M+H for C28H26F2N2O5S).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07528157B2
出典データセットuspto-grants-2009_05
ORD IDord-c34f0852176a4984b1f9d759be30080c
出典メモuspto-grants-2009_05