2-Chloro-6-phenoxybenzylamine → HCID 178523054, compound

HRID 2304905Notes

Reaction equation

HRID 2304905 reaction equation
[NH:1]1[C:5]2[CH2:6][CH2:7][CH:8]([C:10]([OH:12])=O)[CH2:9][C:4]=2[N:3]=[CH:2]1.[Cl:13][C:14]1[CH:21]=[CH:20][CH:19]=[C:18]([O:22][C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[C:15]=1[CH2:16][NH2:17]>>[Cl:13][C:14]1[CH:21]=[CH:20][CH:19]=[C:18]([O:22][C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[C:15]=1[CH2:16][NH:17][C:10]([CH:8]1[CH2:7][CH2:6][C:5]2[NH:1][CH:2]=[N:3][C:4]=2[CH2:9]1)=[O:12]

Participants

3

Reactant 2

HCID 27772062-Chloro-6-phenoxybenzylamineHCID 178524172HCID 178524172, compound

Product 1

HCID 178523054HCID 178523054, compound

Procedure

83 mg of the title compound was prepared from 4,5,6,7-tetrahydro-1H-benzimidazole-5-carboxylic acid and 2-chloro-6-phenoxybenzylamine by a similar procedure as described in Example 1.

Sources & evidence

ORD record
ord-3e077a3aead94823a56ef9821ba3749b
Source dataset
uspto-grants-2002_08
Patent number
US06437147B1

Reaction notes

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