2-Chlorobenzylamine → HCID 178478037, compound

HRID 710507Notes

Reaction equation

HRID 710507 reaction equation
O1[CH:5]=[N:4][N:3]=[C:2]1[C:6]1[CH:14]=[CH:13][C:9]2[N:10]=[CH:11][NH:12][C:8]=2[CH:7]=1.[Cl:15][C:16]1[CH:23]=[CH:22][CH:21]=[CH:20][C:17]=1[CH2:18][NH2:19]>>[Cl:15][C:16]1[CH:23]=[CH:22][CH:21]=[CH:20][C:17]=1[CH2:18][N:19]1[CH:5]=[N:4][N:3]=[C:2]1[C:6]1[CH:14]=[CH:13][C:9]2[NH:10][CH:11]=[N:12][C:8]=2[CH:7]=1

Participants

3

Reactant 2

HCID 666482-ChlorobenzylamineHCID 58433284HCID 58433284, compound

Product 1

HCID 178478037HCID 178478037, compound

Procedure

The compound was synthesized starting from 5-(1,3,4-oxadiazol-2-yl)benzimidazole (186 mg, 1 mmol) and 2-chlorobenzylamine (0.5 ml) as described above; yield: 0.089 g (28.8%);

Workup

  1. customThe compound was synthesized

Sources & evidence

ORD record
ord-31f9ab709a9e412fa340a85b65d01fa5
Source dataset
uspto-grants-2015_11
Patent number
US09181233B2

Reaction notes

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