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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 20582생성일: 2026년 10월 25일

Diisopropylethylamine → 3-[4-(azetidin-1-ylcarbonyl)-2-fluorophenoxy]-5-((1S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethoxy)-N-(3-methyl-1,2,4-thiadiazol-5-yl)benzamide

https://huagongshe.com/reaction/20582

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물5-Amino-3-methyl-1,2,4-thiadiazoleHCID 350639—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물3-[4-(azetidin-1-ylcarbonyl)-2-fluorophenoxy]-5-((1S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethoxy)benzoic acidHCID 59346909—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물3-[4-(azetidin-1-ylcarbonyl)-2-fluorophenoxy]-5-((1S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethoxy)-N-(3-methyl-1,2,4-thiadiazol-5-yl)benzamideHCID 5934688299.5%

반응 단계

DIPEA (0.8 mL, 4.77 mmol) was added to a suspension of 3-[4-(azetidin-1-ylcarbonyl)-2-fluorophenoxy]-5-((1S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethoxy)benzoic acid (800 mg, 1.59 mmol), HATU (787 mg, 2.07 mmol) and 5-amino-3-methyl-1,2,4 thiadiazole (549 mg, 4.77 mmol) in DMF (110 mL). The resulting mixture was stirred at ambient temperature for 16 hours, water (150 mL) was added and the mixture extracted with ethyl acetate. The extracts were combined, washed with brine, dried (MgSO4), filtered and evaporated in vacuo to give the crude product which was chromatographed on silica, eluting with 75% ethyl acetate in isohexane, to give the desired compound (950 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745475B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-0a500e55f03744d7a6fde67ddd75244f
출처 메모uspto-grants-2010_06