2-(2-Bromoethyl)-1H-indole → HCID 16042145, compound

HRID 499692Notes

Reaction equation

HRID 499692 reaction equation
[N:1]12[CH2:7][C:4]([C:8]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=3)[C:9]#[N:10])([CH2:5][CH2:6]1)[CH2:3][CH2:2]2.[Br:23][CH2:24][CH2:25][C:26]1[NH:27][C:28]2[C:33]([CH:34]=1)=[CH:32][CH:31]=[CH:30][CH:29]=2>>[Br-:23].[C:9]([C:8]([C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)([C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=1)[C:4]12[CH2:7][N+:1]([CH2:24][CH2:25][C:26]3[NH:27][C:28]4[C:33]([CH:34]=3)=[CH:32][CH:31]=[CH:30][CH:29]=4)([CH2:6][CH2:5]1)[CH2:2][CH2:3]2)#[N:10]

Participants

3

Reactant 2

HCID 222626702-(2-Bromoethyl)-1H-indoleHCID 42625857HCID 42625857, compound

Product 1

HCID 16042145HCID 16042145, compoundYield 43.6%

Procedure

Following the general procedure outlined in Example 24, 1-azabicyclo[2.2.1]hept-4-yl(diphenyl)acetonitrile (0.044 g, 0.152 mmol) and 2-(2-bromoethyl)-1H-indole (0.0494 g, 0.220 mmol) in 2CH3CN/3CHCl3 (3.5 mL) were reacted to give the desired product (0.0340 g, 43.4%). EI-MS m/z 432 (M+) Rt (1.94 min).

Workup

  1. customwere reacted

Sources & evidence

ORD record
ord-bda9cd49c64048a1a8605f44e109bc05
Source dataset
uspto-grants-2010_08
Patent number
US07767691B2

Reaction notes

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