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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 386819생성일: 2026년 10월 26일

Diisopropylethylamine → 4-amino-N-(3-bromo-4-fluorophenyl)-1,2,5-thiadiazole-3-carboxamide

https://huagongshe.com/reaction/386819

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물4-Amino-1,2,5-thiadiazole-3-carboxylic acidHCID 251763—
반응물Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
반응물3-Bromo-4-fluoroanilineHCID 2779286—
용매Hydrochloric AcidHCID 313—
용매DimethylformamideHCID 6228—
용매Sodium chloride; waterHCID 57417360—
생성물4-amino-N-(3-bromo-4-fluorophenyl)-1,2,5-thiadiazole-3-carboxamideHCID 5855824476.8%

반응 단계

A solution of 4-amino-1,2,5-thiadiazole-3-carboxylic acid (250 mg, 1.7 mmol) and 3-bromo-4-fluoroaniline (393 mg, 2.1 mmol) in N,N-dimethylformamide (5 mL) was treated with O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (784 mg, 2.1 mmol) followed by N,N-diisopropylethylamine (0.36 mL, 2.1 mmol) and stirred for 16 h. The reaction mixture was diluted with brine (50 mL) and 0.1 N HCl (100 mL) and extracted with ethyl acetate (2×150 mL). The combined organic extracts were washed with brine (50 mL), dried with sodium sulfate, filtered, and concentrated. Purification of the crude reaction mixture on silica gel gave the desired product (414 mg, 76%). LCMS for C9H7BrFN4OS(M+H)+: m/z=316.9, 318.8.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08372870B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-3787938b02ad40539dce4a9fc3ff1d74
출처 메모uspto-grants-2013_02