Ethyl 3-chloro-2-methylisonicotinate → 4-methylfuro[2,3-c]pyridin-3(2H)-one O-methyl oxime
Reaction equation
[CH2:1](OC(=O)C1C=CN=C(C)C=1Cl)C.[CH3:14][O:15][N:16]=[C:17]1[C:25]2[C:20](=[CH:21][N:22]=[CH:23][C:24]=2Cl)[O:19][CH2:18]1>>[CH3:14][O:15][N:16]=[C:17]1[C:25]2[C:20](=[CH:21][N:22]=[CH:23][C:24]=2[CH3:1])[O:19][CH2:18]1Participants
3
Procedure
This compound was prepared using a method analogous to that of 3-chloro-2-methylisonicotinic acid ethyl ester (A.2.5.2), 4-chlorofuro[2,3-c]pyridin-3(2H)-one O-methyl oxime replacing 2,3-dichloroisonicotinic acid ethyl ester. Purification by CC using Hept/EtOAc (9/1 to 1/1) gives a white solid;
Workup
- customThis compound was prepared
- customPurification by CC
- customgives a white solid
Sources & evidence
- ORD record
- ord-c3f611547549402cbbf216d14cca8c44
- Source dataset
- uspto-grants-2015_12
- Patent number
- US09221832B2
Reaction notes
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