Hydrochloric Acid → HCID 15812073, 화합물
반응식
O1CCCC1.[CH3:6][C:7]([NH:10][C:11]1[O:12][C:13]([C:20]([O:22]CC)=[O:21])=[C:14]([C:16]([F:19])([F:18])[F:17])[N:15]=1)([CH3:9])[CH3:8].[OH-].[Na+].Cl>O>[CH3:9][C:7]([NH:10][C:11]1[O:12][C:13]([C:20]([OH:22])=[O:21])=[C:14]([C:16]([F:17])([F:19])[F:18])[N:15]=1)([CH3:6])[CH3:8]참가 물질
6
실험 절차
A reaction vessel was charged with 200 ml tetrahydrofuran and 28 g (100 mmol) of ethyl 2-[(1,1dimethylethyl)amino]-4-trifluoromethyl-5-oxazolecarboxylate (prepared by Example 6). With this mixture stirred at ambient temperature, 50% aqueous sodium hydroxide (16 g; 200 mmol) was added followed by 50 ml water as a rinse. The reaction mixture was stirred at ambient temperature for 16 hours. The mixture was then poured into 500 ml of 5% hydrochloric acid. After cooling with an ice bath, the mixture was filtered, washed with water, and then dried to yield 2.4 g of a white powder which was recrystallized from ethyl acetate to a crystalline product (m.p.=256°-258° C.) identified in Table I.
후처리
- stirringThe reaction mixture was stirred at ambient temperature for 16 hours
- temperatureAfter cooling with an ice bath
- filtrationthe mixture was filtered
- washwashed with water
- customdried
출처 및 근거
- ORD 기록
- ord-25e059f518784467abbaad415a2e5cf5
- 출처 데이터셋
- uspto-grants-1991_03
- 특허 번호
- US05000775
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