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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 38090생성일: 2026년 10월 26일

4-Tert-Butylaniline → N-(4-tert-butyl-phenyl)-3-(7-pyridin-4-yl-2,3-dihydro-pyrazolo[5,1-b]thiazol-6-yl)-benzamide

https://huagongshe.com/reaction/38090

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참여 물질

역할이름HCID투입량
반응물4-Tert-ButylanilineHCID 69861—
반응물3-(7-Pyridin-4-yl-2,3-dihydro-pyrazolo[5,1-b]thiazol-6-yl)-benzoic acid hydrochlorideHCID 67424684—
용매Ethyl AcetateHCID 8857—
용매Thionyl ChlorideHCID 24386—
생성물N-(4-tert-butyl-phenyl)-3-(7-pyridin-4-yl-2,3-dihydro-pyrazolo[5,1-b]thiazol-6-yl)-benzamideHCID 4670190677.4%

반응 조건

온도60 °C

반응 단계

3-(7-Pyridin-4-yl-2,3-dihydro-pyrazolo[5,1-b]thiazol-6-yl)-benzoic acid hydrochloride (45 mg, 0.125 mmol) was dissolved in thionylchloride (1 mL) and stirred at 60° C. for 1 hour. The solvent was distilled and the residue was taken up with toluene, evaporated to dryness and dried under high vacuum for 1 h. The acid chloride was then dissolved in dry pyridine (1 mL) under nitrogen and 4-tert-butylaniline (0.030 mL, 0.187 mmol, 1.5 eq) was added. The mixture was stirred at room temperature for 1 h and then diluted with ethyl acetate and washed with saturated aqueous NaHCO3 and brine. The organic layer was dried over Na2SO4 and concentrated under reduced pressure. The crude product was purified by chromatography on silica gel (eluant DCM/EtOH 95:5 to give 44 mg of N-(4-tert-butyl-phenyl)-3-(7-pyridin-4-yl-2,3-dihydro-pyrazolo[5,1-b]thiazol-6-yl)-benzamide as a white solid (77%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524707B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-60819d40753b43e4ad7a8990ed0dc1c1
출처 메모uspto-grants-2013_09