Phosgene → HCID 49779586, compound
Reaction equation
[NH2:1][C:2]1[CH:3]=[CH:4][C:5]([O:8][CH3:9])=[N:6][CH:7]=1.[C:10](Cl)(Cl)=[O:11].Cl.[CH3:15][N:16]1[CH2:21][CH2:20][N:19]([C:22]2[CH:27]=[C:26]([C:28]3[CH:37]=[C:36]4[C:31]([CH2:32][CH2:33][NH:34][CH2:35]4)=[CH:30][CH:29]=3)[N:25]=[C:24]([NH2:38])[N:23]=2)[CH2:18][CH2:17]1>>[NH2:38][C:24]1[N:25]=[C:26]([C:28]2[CH:37]=[C:36]3[C:31]([CH2:32][CH2:33][N:34]([C:10]([NH:1][C:2]4[CH:7]=[N:6][C:5]([O:8][CH3:9])=[CH:4][CH:3]=4)=[O:11])[CH2:35]3)=[CH:30][CH:29]=2)[CH:27]=[C:22]([N:19]2[CH2:18][CH2:17][N:16]([CH3:15])[CH2:21][CH2:20]2)[N:23]=1Participants
4
Procedure
This compound was prepared by using procedures analogous to those described for the synthesis of Example 40 starting from 5-amino-2-methoxypyridine (Aldrich, Cat. #A61209), phosgene and 4-(4-methylpiperazin-1-yl)-6-(1,2,3,4-tetrahydroisoquinolin-7-yl)pyrimidin-2-amine HCl salt. Analytic LCMS (M+H)+: m/z=475.2.
Workup
- customThis compound was prepared
Sources & evidence
- ORD record
- ord-811f8db6ffdc47588679b664e4ccee68
- Source dataset
- uspto-grants-2013_07
- Patent number
- US08481732B2
Reaction notes
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