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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1192076생성일: 2026년 10월 26일

Isopropylamine → 5-[(3,5-dichloro-4-pyridyl)sulfanyl]-N-isopropyl-4-nitro-thiophene-2-carboxamide

https://huagongshe.com/reaction/1192076

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참여 물질

역할이름HCID투입량
반응물IsopropylamineHCID 6363—
반응물TriethylamineHCID 8471—
반응물5-((3,5-Dichloropyridin-4-yl)thio)-4-nitrothiophene-2-carboxylic acidHCID 60207317—
반응물Chloro-1,1,3,3-tetramethyluronium hexachloroantimonateHCID 86664723—
용매DichloromethaneHCID 6344—
생성물5-[(3,5-dichloro-4-pyridyl)sulfanyl]-N-isopropyl-4-nitro-thiophene-2-carboxamideHCID 4693242257.9%

반응 단계

Chloro-1,1,3,3-tetramethyluronium hexachloroantimonate (47 mg, 0.1 mmol) was added to a suspension of 5-[(3,5-dichloro-4-pyridyl)sulfanyl]-4-nitro-thiophene-2-carboxylic acid (39 mg, 0.11 mmol) in dichloromethane (1 mL) and the mixture was stirred at ambient temperature for 10 min. A solution of isopropylamine (9 mg, 0.12 mmol) and triethylamine (12 mg, 0.12 mmol) in dichloromethane (0.5 mL) was added to the above mixture and was stirred at ambient temperature for over night. After passing through a ISOLUTE™ PE-AX cartridge to remove excess amines, the resulting mixture was concentrated and the residue was purified by reverse-phase HPLC to afford the title product as a white solid (25 mg, 49% yield). 1H NMR (300 MHz, d6-DMSO) δ: 9.0 (2H, s), 8.65 (1H, d), 8.50 (1H, s), 4.0 (1H, m), 1.25 (6H, d). MS m/z: 391.70, 393.80 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08680139B2
출처 데이터셋uspto-grants-2014_03
ORD IDord-0c7ac7762bf64e229dcb91c43cb02e4a
출처 메모uspto-grants-2014_03