반응 #92610
ord-c4bb597513e8498b81f19dd0b55f5f5b
반응 방정식
5-amino-1-(2-bromo-5-nitrophenyl)-3-(4-phenoxyphenyl)-1H-pyrazole-4-carbonitrile
phosphorous acid
→
crude product
5-Amino-1-(2-bromo-5-nitrophenyl)-3-(4-phenoxyphenyl)-1H-pyrazole-4-carboxamide
시약
없음
반응 조건
온도
100°CELSIUS
상세 조건
See reaction.notes.procedure_details.
후처리
- 1기타was consumed
- 2온도The reaction was cooled to room temperature
- 3기타partitioned between water (40 mL) and EA (40 mL)
- 4기타Organic layer was separated from aqueous layer
- 5추출The aqueous phase was then extracted with EA (20 mL)
- 6세척The combined organic layers were washed with brine (50 mL)
- 7건조dried over Na2SO4
- 8농축concentrated
실험 절차
A mixture of 5-amino-1-(2-bromo-5-nitrophenyl)-3-(4-phenoxyphenyl)-1H-pyrazole-4-carbonitrile (137 mg, 0.287 mmol) in phosphorous acid (85 wt. % in H2O, 10 mL) was stirred at 100° C. for 1 hr, until TLC and LCMS analysis showed that most of starting material was consumed. The reaction was cooled to room temperature and partitioned between water (40 mL) and EA (40 mL). Organic layer was separated from aqueous layer. The aqueous phase was then extracted with EA (20 mL). The combined organic layers were washed with brine (50 mL), dried over Na2SO4 and concentrated to get the crude product (149 mg) which was used in next step without further purification. MS (ESI) m/e [M+1]+494, 496.