4-Ethynyl-N,N-dimethylaniline → HCID 46892656, compound

HRID 1944038Notes

Reaction equation

HRID 1944038 reaction equation
[N:1]([CH:4]1[CH2:23][N:8]2[C:9]3[C:14]([C:15]([CH2:16][C:17]([O:19]CCC)=[O:18])=[C:7]2[CH2:6][CH2:5]1)=[CH:13][CH:12]=[CH:11][CH:10]=3)=[N+:2]=[N-:3].[C:24]([C:26]1[CH:34]=[CH:33][C:29]([N:30]([CH3:32])[CH3:31])=[CH:28][CH:27]=1)#[CH:25]>>[CH3:31][N:30]([CH3:32])[C:29]1[CH:33]=[CH:34][C:26]([C:24]2[N:3]=[N:2][N:1]([CH:4]3[CH2:23][N:8]4[C:9]5[C:14]([C:15]([CH2:16][C:17]([OH:19])=[O:18])=[C:7]4[CH2:6][CH2:5]3)=[CH:13][CH:12]=[CH:11][CH:10]=5)[CH:25]=2)=[CH:27][CH:28]=1

Participants

3

Reactant 2

HCID 51918844-Ethynyl-N,N-dimethylanilineHCID 59487226Propyl (7-azido-6,7,8,9-tetrahydropyrido[1,2-a]indol-10-yl)acetate

Product 1

HCID 46892656HCID 46892656, compound

Procedure

The title compound was prepared using procedures described in EXAMPLE 1 from propyl (7-azido-6,7,8,9-tetrahydropyrido[1,2-a]indol-10-yl)acetate and 4-ethynyl-N,N-dimethylaniline. MS (+ESI) m/z: 416.2.

Sources & evidence

ORD record
ord-58fc7f1d66b1481eb9fac73db38fd52f
Source dataset
uspto-grants-2013_03
Patent number
US08394819B2

Reaction notes

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