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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 244635생성일: 2026년 10월 24일

Diisopropylethylamine → N-(6-bromo-1H-indazol-4-yl)-2-methyl-1,3-thiazole-4-carboxamide

https://huagongshe.com/ko/reaction/244635

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물2-Methyl-1,3-thiazole-4-carboxylic acidHCID 284728—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물6-Bromo-1H-indazol-4-amineHCID 24728063—
용매DimethylformamideHCID 6228—
생성물N-(6-bromo-1H-indazol-4-yl)-2-methyl-1,3-thiazole-4-carboxamideHCID 5825575018.9%

반응 조건

온도20 °C

반응 단계

2-Methyl-1,3-thiazole-4-carboxylic acid (4.59 g) (available from Maybridge), HATU (13.41 g) and DIPEA (16.80 ml) were stirred in DMF (140 ml) for 30 min at 20° C. 6-Bromo-1H-indazol-4-amine (3.4 g) (available from Sinova) was added and the reaction stirred at 20° C. for 2 days. The solvent was reduced to ˜40 ml and the reaction mixture was applied across 5×70 g aminopropyl SPE cartridges and left to stand for 3 h. The cartridges were eluted with DCM:methanol (1:1) and the combined solvent was evaporated in vacuo. The residue was suspended in DCM:methanol, adsorbed onto Florisil® and purified by chromatography on silica gel (100 g cartridge) eluting with 0-15% gradient of methanol (containing 1% triethylamine) in DCM over 60 min to give title compound (1.02 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08658635B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-a9afde083cea40e7829cf979ee997c21
출처 메모uspto-grants-2014_02