4-Chloro-2-methylpyrimidine → HCID 59239077, compound

HRID 1697902Notes

Reaction equation

HRID 1697902 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][C@@H:24]3[CH3:29])[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].[CH3:30][C:31]1[N:36]=[C:35](Cl)[CH:34]=[CH:33][N:32]=1>>[CH2:1]([NH:3][C:4]([NH:6][C:7]1[CH:8]=[CH:9][C:10]([C:13]2[N:14]=[C:15]([N:23]3[CH2:28][CH2:27][O:26][CH2:25][C@@H:24]3[CH3:29])[C:16]3[CH2:22][CH2:21][N:20]([C:33]4[CH:34]=[CH:35][N:36]=[C:31]([CH3:30])[N:32]=4)[CH2:19][C:17]=3[N:18]=2)=[CH:11][CH:12]=1)=[O:5])[CH3:2]

Participants

3

Reactant 2

HCID 4244474-Chloro-2-methylpyrimidineHCID 46913570Urea, N-ethyl-N'-[4-[5,6,7,8-tetrahydro-4-[(3S)-3-Methyl-4-Morpholinyl]pyrido[3,4-d]pyriMidin-2-yl]phenyl]-

Product 1

HCID 59239077HCID 59239077, compound

Procedure

Compound (dv) was prepared according to the procedure described in Example 2 by reacting (S)-1-ethyl-3-(4-(4-(3-methylmorpholino)-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidin-2-yl)phenyl)urea with 2-methyl-4-chloropyrimidin. LC-MS: m/z=+489 (M+H)+.

Workup

  1. customCompound (dv) was prepared

Sources & evidence

ORD record
ord-52b42fde6824455ea9c9c8d2d60907ab
Source dataset
uspto-grants-2012_04
Patent number
US08163763B2

Reaction notes

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