5-Chloro-3-methoxy-pyridine-2-carboxylic acid → 4-Chloro-7-methoxypyrido(3,2-d)pyrimidine
Reaction equation
[Cl:1]C1C=C(OC)C(C(O)=O)=NC=1.[CH3:13][O:14][C:15]1[CH:24]=[N:23][C:22]2[C:21](=O)[N:20]=[CH:19][NH:18][C:17]=2[CH:16]=1>>[Cl:1][C:21]1[C:22]2[N:23]=[CH:24][C:15]([O:14][CH3:13])=[CH:16][C:17]=2[N:18]=[CH:19][N:20]=1Participants
3
Procedure
Using an analogous reaction to that described for Intermediate 14, step 3, 7-methoxypyrido[3,2-d]pyrimidin-4(1H)-one was converted to the title compound. LC/MS (ESI+) m/z=196 (M+H).
Workup
- customan analogous reaction to
Sources & evidence
- ORD record
- ord-68cdb2d555de43d191cd428075329bde
- Source dataset
- uspto-grants-2016_03
- Patent number
- US09296734B2
Reaction notes
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