Methyl iodide → HCID 23470325, compound

HRID 427162Notes

Reaction equation

HRID 427162 reaction equation
CN(C)C1CC2C3C(=CC(C)=CC=3C)NC=2CC1.[H-].[Na+].CI.Cl.[CH3:24][N:25]([CH3:42])[CH:26]1[CH2:38][C:37]2[C:36]3[C:31](=[CH:32][C:33]([CH3:40])=[CH:34][C:35]=3[CH3:39])[N:30]([CH3:41])[C:29]=2[CH2:28][CH2:27]1>CN(C)C=O>[CH3:42][N:25]([CH3:24])[CH:26]1[CH2:38][C:37]2[C:36]3[C:31](=[CH:32][C:33]([CH3:40])=[CH:34][C:35]=3[CH3:39])[N:30]([CH3:41])[C:29]=2[CH2:28][CH2:27]1

Participants

6

Reactant 4

HCID 6328Methyl iodideHCID 24758Sodium hydrideHCID 12361835N,N,5,7-Tetramethyl-2,3,4,9-tetrahydro-1H-carbazol-3-amineHCID 23470460HCID 23470460, compound

Product 1

HCID 23470325HCID 23470325, compound

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

Following a procedure similar to that described in Example 253 and using 10.3 g. of 3-(dimethylamino)-5,7-dimethyl-1,2,3,4-tetrahydrocarbazole (Example 221), 7.02 g. of sodium hydride, 6.65 g. of methyl iodide, and 70 ml. of dimethylformamide there was obtained 5.4 g. of 3-(dimethylamino)-5,7,9-trimethyl-1,2,3,4-tetrahydrocarbazole hydrochloride, m.p. 320°-322° C.

Sources & evidence

ORD record
ord-c7b9fd0c85584c2cb40ace47a298effd
Source dataset
uspto-grants-1979_10
Patent number
US04172834

Reaction notes

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