반응식
[CH3:1][Si](Cl)(C)C.[I:6][C:7]1[CH:8]=[C:9]([CH:12]=[CH:13][CH:14]=1)[CH:10]=O.[CH:15]([NH2:17])=[O:16].[C:18]1(C)[C:19]([S:24]([OH:26])=[O:25])=[CH:20][CH:21]=[CH:22][CH:23]=1>CC#N.C1(C)C=CC=CC=1.O.COC(C)(C)C>[I:6][C:7]1[CH:8]=[C:9]([CH:10]([NH:17][CH:15]=[O:16])[S:24]([C:19]2[CH:18]=[CH:23][C:22]([CH3:1])=[CH:21][CH:20]=2)(=[O:25])=[O:26])[CH:12]=[CH:13][CH:14]=1참가 물질
반응물 4
생성물 1
시약·촉매·용매 4
반응 조건
- 온도
- 50 °C
실험 절차
Trimethylsilylchloride (9.1 mL) was added to a stirred solution of 3-iodobenzaldehyde (15.1 g) and formamide (6.5 mL) in MeCN (34 mL) and toluene (34 mL) under an inert atmosphere. The reaction was then heated at 50° C. for 5 hours. Toluene sulfinic acid (15.3 g) was added and the reaction mixture was heated at 50° C. for a fisher 5 hours. The reaction mixture was cooled to ambient temperature, methyl t-butylether (55 mL) was added and stirred for 5 minutes. Water (275 mL) was added, the reaction cooled to 0° C. and stirred for 1 hour. The solid was filtered and the reaction flask was washed with MTBE (2×35 mL) and poured over the filtered cake. The solid was dried in a vacuum oven at 60° C. for 10 hours to afford impure title compound as a solid (14 g, 51%) which was used without further purification. A small sample was crystallised from EtOH;
후처리
- temperaturethe reaction mixture was heated at 50° C. for a fisher 5 hours
- temperatureThe reaction mixture was cooled to ambient temperature
- temperaturethe reaction cooled to 0° C.
- stirringstirred for 1 hour
- filtrationThe solid was filtered
- washthe reaction flask was washed with MTBE (2×35 mL)
- additionpoured over the filtered cake
- customThe solid was dried in a vacuum oven at 60° C. for 10 hours
출처 및 근거
- ORD 기록
- ord-6f7c7740c4974382bd848d9d695a005a
- 출처 데이터셋
- uspto-grants-2008_09
- 특허 번호
- US07427616B2
연결된 노트
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