3-(Chloromethyl)-5-[3-(trifluoromethyl)phenyl]-1,2,4-oxadiazole → 4-Chloro-2-methyl-1-({5-[3-(trifluoromethyl)phenyl]-1,2,4-oxadiazol-3-yl}methyl)-1H-indole-5-carbonitrile

HRID 913599Notes

Reaction equation

HRID 913599 reaction equation
[Cl:1][C:2]1[C:10]([C:11]#[N:12])=[CH:9][CH:8]=[C:7]2[C:3]=1[CH:4]=[C:5]([CH3:13])[NH:6]2.Cl[CH2:15][C:16]1[N:20]=[C:19]([C:21]2[CH:26]=[CH:25][CH:24]=[C:23]([C:27]([F:30])([F:29])[F:28])[CH:22]=2)[O:18][N:17]=1>>[Cl:1][C:2]1[C:10]([C:11]#[N:12])=[CH:9][CH:8]=[C:7]2[C:3]=1[CH:4]=[C:5]([CH3:13])[N:6]2[CH2:15][C:16]1[N:20]=[C:19]([C:21]2[CH:26]=[CH:25][CH:24]=[C:23]([C:27]([F:30])([F:28])[F:29])[CH:22]=2)[O:18][N:17]=1

Participants

3

Reactant 2

HCID 27366223-(Chloromethyl)-5-[3-(trifluoromethyl)phenyl]-1,2,4-oxadiazoleHCID 674048784-chloro-2-methyl-1H-indole-5-carbonitrile

Product 1

HCID 578003164-Chloro-2-methyl-1-({5-[3-(trifluoromethyl)phenyl]-1,2,4-oxadiazol-3-yl}methyl)-1H-indole-5-carbonitrile

Procedure

Synthesized as described in Example 4 from 4-chloro-2-methyl-1H-indole-5-carbonitrile and 3-(chloromethyl)-5-[3-(trifluoromethyl)phenyl]-1,2,4-oxadiazole: 1H NMR (400 MHz, DMSO-d6) δ 8.31 (d, J=7.9 Hz, 1 H), 8.24 (s, 1 H), 8.06 (d, J=7.6 Hz, 1 H), 7.94 (d, J=1.1 Hz, 1 H), 7.87-7.79 (m, 2 H), 7.59 (dd, J=8.5, 1.5 Hz, 1 H), 5.85 (s, 2 H), 2.47 (s, 3 H); MS (ES) m/z 417 (M+1).

Workup

  1. customSynthesized

Sources & evidence

ORD record
ord-bb0049bac6104d0398b2b91c5e2b21e5
Source dataset
uspto-grants-2011_09
Patent number
US08026262B2

Reaction notes

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