1-Cyanocyclopropanecarboxylic acid → HCID 59239286, compound
Reaction equation
[CH2:1]([NH:3][C:4]([NH:6][C:7]1[CH:12]=[CH:11][C:10]([C:13]2[N:14]=[C:15]([N:23]3[CH2:28][CH2:27][O:26][CH2:25][CH2:24]3)[C:16]3[CH2:22][CH2:21][NH:20][CH2:19][C:17]=3[N:18]=2)=[CH:9][CH:8]=1)=[O:5])[CH3:2].[C:29]([C:31]1([C:34](O)=[O:35])[CH2:33][CH2:32]1)#[N:30]>>[C:29]([C:31]1([C:34]([N:20]2[CH2:21][CH2:22][C:16]3[C:15]([N:23]4[CH2:24][CH2:25][O:26][CH2:27][CH2:28]4)=[N:14][C:13]([C:10]4[CH:9]=[CH:8][C:7]([NH:6][C:4]([NH:3][CH2:1][CH3:2])=[O:5])=[CH:12][CH:11]=4)=[N:18][C:17]=3[CH2:19]2)=[O:35])[CH2:33][CH2:32]1)#[N:30]Participants
3
Procedure
Compound fe was prepared according to the procedure described in Example 213 by reacting 1-ethyl-3-(4-(4-morpholino-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidin-2-yl)phenyl)urea with 1-cyanocyclopropanecarboxylic acid. LC-MS: m/z=+476 (M+H)−.
Workup
- customCompound fe was prepared
Sources & evidence
- ORD record
- ord-01a4b5b891374f9caa5181a78573d849
- Source dataset
- uspto-grants-2012_04
- Patent number
- US08163763B2
Reaction notes
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