Chlorotrimethylsilane → HCID 9982497, compound

HRID 2357457Notes

Reaction equation

HRID 2357457 reaction equation
[CH3:1][N:2]([CH3:33])[C:3]1([C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=2)[CH2:8][CH2:7][C:6](=[CH:9][C:10]([N:12]2[CH2:17][CH2:16][CH:15]([C:18]3[C:26]4[C:21](=[CH:22][CH:23]=[CH:24][CH:25]=4)[NH:20][CH:19]=3)[CH2:14][CH2:13]2)=[O:11])[CH2:5][CH2:4]1.[Cl:34][Si](C)(C)C>CC(CC)=O>[ClH:34].[CH3:33][N:2]([CH3:1])[C:3]1([C:27]2[CH:28]=[CH:29][CH:30]=[CH:31][CH:32]=2)[CH2:8][CH2:7][C:6](=[CH:9][C:10]([N:12]2[CH2:17][CH2:16][CH:15]([C:18]3[C:26]4[C:21](=[CH:22][CH:23]=[CH:24][CH:25]=4)[NH:20][CH:19]=3)[CH2:14][CH2:13]2)=[O:11])[CH2:5][CH2:4]1

Participants

4

Procedure

2-(4-dimethylamino-4-phenylcyclohexylidene)-1-[4-(1H-indol-3-yl)-piperidine-1-yl]ethanone (344 mg, 0.779 mmole) was dissolved in ethyl methyl ketone (10 ml) and chlorotrimethylsilane (0.15 ml, 1.2 mmole) was added. After 45 minutes the hydrochloride was isolated as a beige-coloured solid with an m.p. of 178-180° C. in a yield of 65% (242 mg) (Example 26).

Sources & evidence

ORD record
ord-09465198bcf34c23b32c5995b848edb9
Source dataset
uspto-grants-2010_07
Patent number
US07759385B2

Reaction notes

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