Benzenemethanamine, 3,4-dichloro- → HCID 25217712, compound

HRID 1966533Notes

Reaction equation

HRID 1966533 reaction equation
Cl[C:2]1[C:11]2[C:6](=[C:7]([O:12][C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][N:14]=3)[CH:8]=[CH:9][CH:10]=2)[N:5]=[C:4]([CH3:19])[CH:3]=1.[Cl:20][C:21]1[CH:22]=[C:23]([CH:26]=[CH:27][C:28]=1[Cl:29])[CH2:24][NH2:25]>>[Cl:20][C:21]1[CH:22]=[C:23]([CH:26]=[CH:27][C:28]=1[Cl:29])[CH2:24][NH:25][C:2]1[C:11]2[C:6](=[C:7]([O:12][C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][N:14]=3)[CH:8]=[CH:9][CH:10]=2)[N:5]=[C:4]([CH3:19])[CH:3]=1

Participants

3

Reactant 2

HCID 1608Benzenemethanamine, 3,4-dichloro-HCID 68497008HCID 68497008, compound

Product 1

HCID 25217712HCID 25217712, 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-(pyridin-2-yloxy)-quinoline and 3,4-dichlorobenzylamine.

Workup

  1. customPreparation

Sources & evidence

ORD record
ord-a317722bdd64472bb6b938e423ff29e8
Source dataset
uspto-grants-2013_04
Patent number
US08420670B2

Reaction notes

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