Trimethylsilyl isocyanate → HCID 57670157, compound

HRID 1894564Notes

Reaction equation

HRID 1894564 reaction equation
[C:1]([C:5]1[N:10]=[CH:9][C:8]([C:11]2[N:12]([C:32]([N:34]3[CH2:39][CH2:38][NH:37][CH2:36][CH2:35]3)=[O:33])[C@@:13]([C:25]3[CH:30]=[CH:29][C:28]([Cl:31])=[CH:27][CH:26]=3)([CH3:24])[C@@:14]([C:17]3[CH:22]=[CH:21][C:20]([Cl:23])=[CH:19][CH:18]=3)([CH3:16])[N:15]=2)=[C:7]([O:40][CH2:41][CH3:42])[CH:6]=1)([CH3:4])([CH3:3])[CH3:2].C[Si]([N:47]=[C:48]=[O:49])(C)C>>[C:1]([C:5]1[N:10]=[CH:9][C:8]([C:11]2[N:12]([C:32]([N:34]3[CH2:39][CH2:38][N:37]([C:48]([NH2:47])=[O:49])[CH2:36][CH2:35]3)=[O:33])[C@@:13]([C:25]3[CH:30]=[CH:29][C:28]([Cl:31])=[CH:27][CH:26]=3)([CH3:24])[C@@:14]([C:17]3[CH:18]=[CH:19][C:20]([Cl:23])=[CH:21][CH:22]=3)([CH3:16])[N:15]=2)=[C:7]([O:40][CH2:41][CH3:42])[CH:6]=1)([CH3:2])([CH3:3])[CH3:4]

Participants

3

Procedure

In a manner analogous to the method described in example 160, [(4S,5R)-2-(6-tert-butyl-4-ethoxy-pyridin-3-yl)-4,5-bis-(4-chloro-phenyl)-4,5-dimethyl-4,5-dihydro-imidazol-1-yl]-piperazin-1-yl-methanone (example 185) was reacted with trimethylsilyl isocyanate (TCI-US) to give the title compound. HR-MS (ES, m/z) calculated for C34H41Cl2N6O3 [(M+H)+] 651.2612, observed 651.2608.

Sources & evidence

ORD record
ord-82dc8c64bd0744e798b7d9b3e1793e2c
Source dataset
uspto-grants-2013_08
Patent number
US08513239B2

Reaction notes

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