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HRID 1192076作成日:2026年10月27日

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

https://huagongshe.com/reaction/1192076

反応式

関与物質

役割名称HCID仕込み量
反応物IsopropylamineHCID 6363—
反応物TriethylamineHCID 8471—
反応物5-((3,5-Dichloropyridin-4-yl)thio)-4-nitrothiophene-2-carboxylic acidHCID 60207317—
反応物Chloro-1,1,3,3-tetramethyluronium hexachloroantimonateHCID 86664723—
溶媒DichloromethaneHCID 6344—
生成物5-[(3,5-dichloro-4-pyridyl)sulfanyl]-N-isopropyl-4-nitro-thiophene-2-carboxamideHCID 4693242257.9%

反応手順

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]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08680139B2
出典データセットuspto-grants-2014_03
ORD IDord-0c7ac7762bf64e229dcb91c43cb02e4a
出典メモuspto-grants-2014_03