Glycolic Acid → (5-ethoxy-3-methyl-3H-imidazo[4,5-b]pyridin-2-yl)methanol
반응식
[NH2:1][C:2]1[C:3]([NH:11][CH3:12])=[N:4][C:5]([O:8][CH2:9][CH3:10])=[CH:6][CH:7]=1.[C:13]([OH:17])(=O)[CH2:14]O>>[CH2:9]([O:8][C:5]1[N:4]=[C:3]2[N:11]([CH3:12])[C:14]([CH2:13][OH:17])=[N:1][C:2]2=[CH:7][CH:6]=1)[CH3:10]참가 물질
3
실험 절차
A procedure similar to that described in Preparation 43 was repeated, except that 4.15 g 3-amino-6-ethoxy-2-methylaminopyridine (prepared as described in Preparation 97), and 5.66 g of glycolic acid were used, and that the product was purified by column chromatography through silica gel, using a 10:1 by volume mixture of ethyl acetate and methanol as the eluent, to give 3.20 g of the title compound, melting at 161° C.
후처리
- customA procedure similar to that described in Preparation 43
- customthat the product was purified by column chromatography through silica gel
- additionby volume mixture of ethyl acetate and methanol as the eluent
출처 및 근거
- ORD 기록
- ord-9ee7c56e009d4c0cb8ff320b2ad306b9
- 출처 데이터셋
- uspto-grants-1998_11
- 특허 번호
- US05834501
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