3-(Dimethylamino)pyrrolidine → HCID 68766659, compound

HRID 2391653Notes

Reaction equation

HRID 2391653 reaction equation
CS(O[CH2:6][C:7]1[N:12]=[CH:11][C:10]2[N:13]=[CH:14][N:15]([C:16]3[S:17][C:18]([C:34](=[O:36])[NH2:35])=[C:19]([O:21][C@@H:22]([C:24]4[CH:29]=[CH:28][CH:27]=[CH:26][C:25]=4[C:30]([F:33])([F:32])[F:31])[CH3:23])[CH:20]=3)[C:9]=2[CH:8]=1)(=O)=O.[CH3:37][N:38]([CH3:44])[CH:39]1[CH2:43][CH2:42][NH:41][CH2:40]1>ClCCl>[CH3:37][N:38]([CH3:44])[CH:39]1[CH2:43][CH2:42][N:41]([CH2:6][C:7]2[N:12]=[CH:11][C:10]3[N:13]=[CH:14][N:15]([C:16]4[S:17][C:18]([C:34]([NH2:35])=[O:36])=[C:19]([O:21][C@@H:22]([C:24]5[CH:29]=[CH:28][CH:27]=[CH:26][C:25]=5[C:30]([F:31])([F:32])[F:33])[CH3:23])[CH:20]=4)[C:9]=3[CH:8]=2)[CH2:40]1

Participants

4

Reactant 2

HCID 27585193-(Dimethylamino)pyrrolidineHCID 86647102[1-(5-carbamoyl-4-{(1R)-1-[2-(trifluoro-methyl)phenyl]ethoxy}-2-thienyl)-1H-imidazo[4,5-c]pyridin-6-yl]methyl methanesulfonate

Product 1

HCID 68766659HCID 68766659, compound

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

In a similar manner as described for example 58, 108 mg of [1-(5-carbamoyl-4-{(1R)-1-[2-(trifluoromethyl)phenyl]ethoxy}-2-thienyl)-1H-imidazo[4,5-c]pyridin-6-yl]methyl methanesulfonate and 114.2 mg of 3-(dimethylamino)pyrrolidine in 2.5 ml dichloromethane give the title compound.

Sources & evidence

ORD record
ord-33d26fd6e78a4cefab163b8ea80fb8d1
Source dataset
uspto-grants-2012_09
Patent number
US08273890B2

Reaction notes

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