6-Bromo-3-methyl[1,3]oxazolo[4,5-b]pyridin-2(3H)-one → 6-Acetyl-2-benzyloxyoxazolo[4,5-b]pyridine
반응식
[CH2:1]([O:8][C:9]1[O:10][C:11]2[C:12]([N:18]=1)=[N:13][CH:14]=[C:15](Br)[CH:16]=2)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.BrC1[CH:21]=[C:22]2[O:28]C(=O)N(C)C2=NC=1>>[C:22]([C:15]1[CH:16]=[C:11]2[O:10][C:9]([O:8][CH2:1][C:2]3[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=3)=[N:18][C:12]2=[N:13][CH:14]=1)(=[O:28])[CH3:21]참가 물질
3
실험 절차
The method of operation is the same as that used for the synthesis of the compound of Example 1 (coupling with 1-ethoxy-1-(trimethylstannyl)ethylene), 2-benzyloxy-6-bromooxazolo[4,5-b]pyridine from Preparation 4 being used instead of the 6-bromo-3-methyloxazolo[4,5-b]pyridin-2(3H)-one from Preparation 2. The yield obtained is 78%. ##STR49##
후처리
- customThe yield obtained
출처 및 근거
- ORD 기록
- ord-54b4091bbb124d768a7411fc5e06240b
- 출처 데이터셋
- uspto-grants-1997_04
- 특허 번호
- US05618819
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