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HRID 72954作成日:2026年10月27日

Cyclopropylamine → 4-(Cyclopropylsulfamoyl)benzoic acid

https://huagongshe.com/reaction/72954

反応式

関与物質

役割名称HCID仕込み量
反応物CyclopropylamineHCID 69828—
反応物4-(Chlorosulfonyl)benzoic acidHCID 82385—
溶媒DichloromethaneHCID 6344—
生成物4-(Cyclopropylsulfamoyl)benzoic acidHCID 113415192%

反応手順

To 4-chlorosulfonylbenzoic acid (10.0 g, 45.3 mmol) in dichloromethane (350 mL) at 0° C. was added cyclopropanamine (15.5 g, 19 mL, 271.9 mmol). The reaction mixture was allowed to warm to room temperature over 16 hours. The solvent was evaporated under reduced pressure. The residue was dissolved in water (150 mL) and acidified using hydrochloric acid. The aqueous layer was extracted with EtOAc (2×200 mL). The organic layer was dried over sodium sulfate, filtered and concentrated in vacuo to give 4-(cyclopropylsulfamoyl)benzoic acid (10.0 g, 92%) as a white solid. ESI-MS m/z calc. 241.0. Found 242.5 (M+1)+; Retention time: 0.84 minutes (3 min run); 1H NMR (400 MHz, DMSO) δ 13.27 (s, 1H), 7.97 (d, J=8.3 Hz, 2H), 7.91 (d, J=2.5 Hz, 1H), 7.75 (d, J=8.3 Hz, 2H), 2.03-1.90 (m, 1H), 0.38-0.28 (m, 2H), 0.23-0.15 (m, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08828996B2
出典データセットuspto-grants-2014_09
ORD IDord-565b84c7b0b54097a5caefa938cf5259
出典メモuspto-grants-2014_09