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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Tert-Butylaniline | HCID 69861 | — |
| 반응물 | 3-(7-Pyridin-4-yl-2,3-dihydro-pyrazolo[5,1-b]thiazol-6-yl)-benzoic acid hydrochloride | HCID 67424684 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 용매 | Thionyl Chloride | HCID 24386 | — |
| 생성물 | N-(4-tert-butyl-phenyl)-3-(7-pyridin-4-yl-2,3-dihydro-pyrazolo[5,1-b]thiazol-6-yl)-benzamide | HCID 46701906 | 77.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08524707B2 |
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| 출처 데이터셋 | uspto-grants-2013_09 |
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| ORD ID | ord-60819d40753b43e4ad7a8990ed0dc1c1 |
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| 출처 메모 | uspto-grants-2013_09 |
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