Hydrochloric Acid → 5-(4-methyl-3-pyridinyl)-1-(3-{(1S,5R)-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hex-3-yl}propyl)-2,4(1H,3H)-pyrimidinedione dihydrochloride

HRID 12809Notes

Reaction equation

HRID 12809 reaction equation
[CH3:1][C:2]1[CH:7]=[CH:6][N:5]=[CH:4][C:3]=1[C:8]1[C:9](=[O:34])[NH:10][C:11](=[O:33])[N:12]([CH2:14][CH2:15][CH2:16][N:17]2[CH2:22][C@H:21]3[C@:19]([C:23]4[CH:28]=[CH:27][C:26]([C:29]([F:32])([F:31])[F:30])=[CH:25][CH:24]=4)([CH2:20]3)[CH2:18]2)[CH:13]=1.[ClH:35]>O1CCOCC1>[ClH:35].[ClH:35].[CH3:1][C:2]1[CH:7]=[CH:6][N:5]=[CH:4][C:3]=1[C:8]1[C:9](=[O:34])[NH:10][C:11](=[O:33])[N:12]([CH2:14][CH2:15][CH2:16][N:17]2[CH2:22][C@H:21]3[C@:19]([C:23]4[CH:24]=[CH:25][C:26]([C:29]([F:32])([F:31])[F:30])=[CH:27][CH:28]=4)([CH2:20]3)[CH2:18]2)[CH:13]=1

Participants

4

Procedure

5-(4-methyl-3-pyridinyl)-1-(3-{(1S,5R)-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hex-3-yl}propyl)-2,4(1H,3H)-pyrimidinedione was suspended in dioxane (2 ml) and treated with a 4N HCl in dioxane solution (2 eq) to give the title compound as a white solid.

Sources & evidence

ORD record
ord-27d30a6915c94cb8bc6831dbaf3796ce
Source dataset
uspto-grants-2010_06
Patent number
US07727988B2

Reaction notes

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