2-Aminobenzonitrile → HCID 22664667, compound

HRID 1835943Notes

Reaction equation

HRID 1835943 reaction equation
[CH3:1][N:2]([CH3:18])[C:3]1[CH:17]=[CH:16][C:6]2[N:7]=[C:8]([CH2:10][C:11]([O:13]CC)=O)[NH:9][C:5]=2[CH:4]=1.[C:19](#[N:27])[C:20]1[C:21](=[CH:23][CH:24]=[CH:25][CH:26]=1)[NH2:22]>>[CH3:18][N:2]([CH3:1])[C:3]1[CH:17]=[CH:16][C:6]2[N:7]=[C:8]([CH2:10][C:11]([NH:22][C:21]3[CH:23]=[CH:24][CH:25]=[CH:26][C:20]=3[C:19]#[N:27])=[O:13])[NH:9][C:5]=2[CH:4]=1

Participants

3

Reactant 2

HCID 729132-AminobenzonitrileHCID 21883426HCID 21883426, compound

Product 1

HCID 22664667HCID 22664667, compound

Procedure

The title compound was synthesized as described in Example 9, Method B using ethyl 2-[5-(dimethylamino)benzimidazol-2-yl]acetate and anthranilonitrile. LC/MS m/z 320.2 (MH+), Rt 1.68 minutes.

Sources & evidence

ORD record
ord-4c887ad763c146ed8564a35633720489
Source dataset
uspto-grants-2004_08
Patent number
US06774237B2

Reaction notes

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