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

HRID 12759Notes

Reaction equation

HRID 12759 reaction equation
[F:1][C:2]([F:32])([F:31])[C:3]1[C:4](=[O:30])[NH:5][C:6](=[O:29])[N:7]([CH2:9][CH2:10][CH2:11][CH2:12][N:13]2[CH2:18][C@H:17]3[C@:15]([C:19]4[CH:24]=[CH:23][C:22]([C:25]([F:28])([F:27])[F:26])=[CH:21][CH:20]=4)([CH2:16]3)[CH2:14]2)[CH:8]=1.[ClH:33]>O1CCOCC1>[ClH:33].[F:32][C:2]([F:1])([F:31])[C:3]1[C:4](=[O:30])[NH:5][C:6](=[O:29])[N:7]([CH2:9][CH2:10][CH2:11][CH2:12][N:13]2[CH2:18][C@H:17]3[C@:15]([C:19]4[CH:24]=[CH:23][C:22]([C:25]([F:28])([F:27])[F:26])=[CH:21][CH:20]=4)([CH2:16]3)[CH2:14]2)[CH:8]=1

Participants

4

Reactant 2

HCID 313Hydrochloric AcidHCID 247591135-(trifluoromethyl)-1-(4-{(1S,5R)-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hex-3-yl}butyl)-2,4(1H,3H)-pyrimidinedione

Product 1

HCID 866159525-(trifluoromethyl)-1-(4-{(1S,5R)-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hex-3-yl}butyl)-2,4(1H,3H)-pyrimidinedione hydrochloride

Reagents, catalysts & solvents 1

HCID 312751,4-DioxaneSolvent

Procedure

5-(trifluoromethyl)-1-(4-{(1S,5R)-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hex-3-yl}butyl)-2,4(1H,3H)-pyrimidinedione was treated with a solution of 4N HCl in dioxane (200 μl) to give the title compound as a yellow solid.

Sources & evidence

ORD record
ord-2336106645ec442db20a116bc5a04bda
Source dataset
uspto-grants-2010_06
Patent number
US07727988B2

Reaction notes

Loading…