N-(azetidin-3-ylcarbamoylmethyl)-3-trifluoromethyl-benzamide → HCID 46241827, compound

HRID 2096160Notes

Reaction equation

HRID 2096160 reaction equation
[OH:1][C:2]1([C:9]2[CH:10]=[N:11][C:12]([O:16][CH3:17])=[C:13]([CH3:15])[CH:14]=2)[CH2:7][CH2:6][C:5](=O)[CH2:4][CH2:3]1.[NH:18]1[CH2:21][CH:20]([NH:22][C:23]([CH2:25][NH:26][C:27](=[O:38])[C:28]2[CH:33]=[CH:32][CH:31]=[C:30]([C:34]([F:37])([F:36])[F:35])[CH:29]=2)=[O:24])[CH2:19]1>>[OH:1][C:2]1([C:9]2[CH:10]=[N:11][C:12]([O:16][CH3:17])=[C:13]([CH3:15])[CH:14]=2)[CH2:7][CH2:6][CH:5]([N:18]2[CH2:21][CH:20]([NH:22][C:23]([CH2:25][NH:26][C:27](=[O:38])[C:28]3[CH:33]=[CH:32][CH:31]=[C:30]([C:34]([F:37])([F:35])[F:36])[CH:29]=3)=[O:24])[CH2:19]2)[CH2:4][CH2:3]1

Participants

3

Reactant 2

HCID 59361594N-(azetidin-3-ylcarbamoylmethyl)-3-trifluoromethyl-benzamideHCID 59361632HCID 59361632, compound

Product 1

HCID 46241827HCID 46241827, compound

Procedure

The title compounds were prepared as white solids from reductive amination of 4-hydroxy-4-(6-methoxy-5-methyl-pyridin-3-yl)-cyclohexanone, as prepared in the previous step, and N-(azetidin-3-ylcarbamoylmethyl)-3-trifluoromethyl-benzamide using the procedure described in Step E of Example 1.

Sources & evidence

ORD record
ord-60949cc9f9df4f479b4c04d3c354b511
Source dataset
uspto-grants-2013_05
Patent number
US08450304B2

Reaction notes

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