반응식
S(Cl)([Cl:3])=O.[CH3:5][C:6]1[N:14]=[C:13]([C:15]([F:18])([F:17])[F:16])[CH:12]=[CH:11][C:7]=1[C:8](O)=[O:9]>C1(C)C=CC=CC=1>[CH3:5][C:6]1[C:7]([C:8]([Cl:3])=[O:9])=[CH:11][CH:12]=[C:13]([C:15]([F:18])([F:17])[F:16])[N:14]=1참가 물질
4
실험 절차
Thionyl chloride (4.35 g, 36.5 mmol) was added to a mixture of 2-methyl-6-trifluoromethyl nicotinic acid (5.00 g, 24.4 mmol) in 75 mL of toluene and the mixture was heated at reflux for 3 hours. The reaction was cooled to room temperature and the solvent was removed under reduced pressure. Excess thionyl chloride was removed by azeotrope with toluene. The resultant acid chloride was used as is in Example 4, Step B.
후처리
- temperaturethe mixture was heated
- temperatureat reflux for 3 hours
- customthe solvent was removed under reduced pressure
- customExcess thionyl chloride was removed by azeotrope with toluene
출처 및 근거
- ORD 기록
- ord-292669329be041e58347e6c40fe1f5c5
- 출처 데이터셋
- uspto-grants-2008_03
- 특허 번호
- US07338978B2
연결된 노트
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