3,4-Difluorobenzylamine → HCID 59474783, compound

HRID 1966548Notes

Reaction equation

HRID 1966548 reaction equation
Cl[C:2]1[C:11]2[C:6](=[C:7]([CH3:12])[CH:8]=[CH:9][CH:10]=2)[N:5]=[C:4]([CH3:13])[CH:3]=1.[F:14][C:15]1[CH:16]=[C:17]([CH:20]=[CH:21][C:22]=1[F:23])[CH2:18][NH2:19]>>[F:14][C:15]1[CH:16]=[C:17]([CH:20]=[CH:21][C:22]=1[F:23])[CH2:18][NH:19][C:2]1[C:11]2[C:6](=[C:7]([CH3:12])[CH:8]=[CH:9][CH:10]=2)[N:5]=[C:4]([CH3:13])[CH:3]=1

Participants

3

Reactant 2

HCID 1235723,4-DifluorobenzylamineHCID 8095564-Chloro-2,8-dimethylquinoline

Product 1

HCID 59474783HCID 59474783, compound

Procedure

Preparation was made using a similar procedure as described in example 1, method 1.3. Starting materials were 4-chloro-2-methyl-8-methylquinoline and 3,4-difluorobenzylamine.

Workup

  1. customPreparation

Sources & evidence

ORD record
ord-00b96b5172c1415192e940917d58ea94
Source dataset
uspto-grants-2013_04
Patent number
US08420670B2

Reaction notes

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