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HRID 386711作成日:2026年10月27日

Benzoic acid, 3-(chlorosulfonyl)-, methyl ester → 3-[(1-tert-Butoxycarbonyl-cyclobutylmethyl)-sulfamoyl]-benzoic acid methyl ester

https://huagongshe.com/reaction/386711

反応式

関与物質

役割名称HCID仕込み量
反応物Benzoic acid, 3-(chlorosulfonyl)-, methyl esterHCID 113339—
反応物Tert-butyl 1-(aminomethyl)cyclobutane-1-carboxylateHCID 66797588—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DichloromethaneHCID 6344—
生成物3-[(1-tert-Butoxycarbonyl-cyclobutylmethyl)-sulfamoyl]-benzoic acid methyl esterHCID 66797535—

反応手順

A solution of 1-aminomethyl-cyclobutanecarboxylic acid tert-butyl ester (step 2) (1.47 g, 7.38 mmol) in DCM (40 ml) was treated with TEA (2.57 ml, 18.44 mmol) followed by methyl 3-(chlorosulfonyl)benzoate (1.91 g, 8.11 mmol) and DMAP (0.09 g, 0.74 mmol). The mixture was stirred at RT for 2 h and then partitioned between DCM and water. The aqueous portion was extracted with DCM and the combined organic extracts were washed with 0.1N HCl, brine, dried over MgSO4 and concentrated in vacuo. Purification of the resulting oil by chromatography on silica eluting with 0-40% EtOAc in iso-hexane afforded the title compound as a colourless oil; 1H NMR (400 MHz, CDCl3) δ 8.56 (1H, s), 8.27 (1H, d), 8.08 (1H, d), 7.64 (1H, t), 5.21 (1H, br t), 3.98 (3H, s), 3.20 (2H, d), 2.37 (2H, m), 1.96 (4H, m), 1.46 (9H, s).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08372845B2
出典データセットuspto-grants-2013_02
ORD IDord-e8c18e980a8440dd91d4abaf57117a64
出典メモuspto-grants-2013_02