Sodium borohydride → HCID 11047852, 화합물
반응식
[CH2:1]([O:8][C:9]1[CH:10]=[C:11]2[C:16](=[CH:17][C:18]=1[F:19])[N:15]=[C:14]([I:20])[C:13]([CH:21]=[O:22])=[CH:12]2)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[BH4-].[Na+]>CO>[CH2:1]([O:8][C:9]1[CH:10]=[C:11]2[C:16](=[CH:17][C:18]=1[F:19])[N:15]=[C:14]([I:20])[C:13]([CH2:21][OH:22])=[CH:12]2)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1참가 물질
4
실험 절차
A suspension of 6-benzyloxy-7-fluoro-2-iodo-3-quinolinecarbaldehyde (obtained according to 1.e, 13 g, 32 mmol) in methanol (100 ml) is treated with sodium borohydride (1.85 g, 48 mmol). After 1 hour of reaction, the reaction medium is concentrated under reduced pressure then taken up with water, filtered, washed with water and ethanol in order to produce, after drying under reduced pressure, 10 g (76%) of a white solid, m.p. 188° C.
후처리
- customAfter 1 hour of reaction
- concentrationthe reaction medium is concentrated under reduced pressure
- filtrationfiltered
- washwashed with water and ethanol in order
- customto produce
- dry with materialafter drying under reduced pressure, 10 g (76%) of a white solid, m.p. 188° C.
출처 및 근거
- ORD 기록
- ord-ea7d5449aba440ba9a6ce7d826699629
- 출처 데이터셋
- uspto-grants-2002_08
- 특허 번호
- US06436951B1
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