2-Chloro-5-ethylpyrimidine → N-Cyclopropyl-N-[1-(5-ethyl-pyrimidin-2-yl)-3-methyl-piperidin-4-yl]-4-oxazol-5-yl-benzamide

HRID 68849

Reaction equation

HRID 68849 reaction equation
[CH:1]1([N:4]([CH:18]2[CH2:23][CH2:22][NH:21][CH2:20][CH:19]2[CH3:24])[C:5](=[O:17])[C:6]2[CH:11]=[CH:10][C:9]([C:12]3[O:16][CH:15]=[N:14][CH:13]=3)=[CH:8][CH:7]=2)[CH2:3][CH2:2]1.Cl[C:26]1[N:31]=[CH:30][C:29]([CH2:32][CH3:33])=[CH:28][N:27]=1>CN1CCCC1=O>[CH:1]1([N:4]([CH:18]2[CH2:23][CH2:22][N:21]([C:26]3[N:31]=[CH:30][C:29]([CH2:32][CH3:33])=[CH:28][N:27]=3)[CH2:20][CH:19]2[CH3:24])[C:5](=[O:17])[C:6]2[CH:7]=[CH:8][C:9]([C:12]3[O:16][CH:15]=[N:14][CH:13]=3)=[CH:10][CH:11]=2)[CH2:3][CH2:2]1

Participants

4

Reactant 2

HCID 35727632-Chloro-5-ethylpyrimidineHCID 68290188HCID 68290188, compound

Product 1

HCID 68351874N-Cyclopropyl-N-[1-(5-ethyl-pyrimidin-2-yl)-3-methyl-piperidin-4-yl]-4-oxazol-5-yl-benzamide

Reagents, catalysts & solvents 1

HCID 13387N-methyl-2-pyrrolidoneSolvent

Procedure

The title compound is prepared from N-cyclopropyl-N-(3-methyl-piperidin-4-yl)-4-oxazol-5-yl-benzamide and 2-chloro-5-ethyl-pyrimidine following a procedure analogous to that described in Example 19 using N-methylpyrrolidinone as solvent. LC (method 3): tR=1.83 min; Mass spectrum (ESI+): m/z=432 [M+H]+.

Sources & evidence

ORD record
ord-8ff19b4de1b04a52abe88db08cbe8a5c
Source dataset
uspto-grants-2014_09
Patent number
US08822471B2

Linked notes

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