Methoxyacetyl chloride → HCID 58579968, compound

HRID 389285Notes

Reaction equation

HRID 389285 reaction equation
Cl.Cl.[CH2:3]([O:5][C:6](=[O:30])[CH2:7][C:8]1[CH:13]=[CH:12][C:11]([O:14][CH3:15])=[C:10]([C:16]2[C:17]([CH2:26][NH:27][CH2:28][CH3:29])=[N:18][C:19]3[C:24]([CH:25]=2)=[CH:23][CH:22]=[CH:21][CH:20]=3)[CH:9]=1)[CH3:4].[CH3:31][O:32][CH2:33][C:34](Cl)=[O:35]>>[CH2:3]([O:5][C:6](=[O:30])[CH2:7][C:8]1[CH:13]=[CH:12][C:11]([O:14][CH3:15])=[C:10]([C:16]2[C:17]([CH2:26][N:27]([CH2:28][CH3:29])[C:34](=[O:35])[CH2:33][O:32][CH3:31])=[N:18][C:19]3[C:24]([CH:25]=2)=[CH:23][CH:22]=[CH:21][CH:20]=3)[CH:9]=1)[CH3:4]

Participants

3

Reactant 2

HCID 96623Methoxyacetyl chlorideHCID 131730235HCID 131730235, compound

Product 1

HCID 58579968HCID 58579968, compound

Procedure

Prepared according to the procedure described in Example 5, Step 5, using the following starting materials: [3-(2-ethylaminomethyl-quinolin-3-yl)-4-methoxy-phenyl]-acetic acid ethyl ester, dihydrochloride and methoxyacetyl chloride.

Workup

  1. customPrepared

Sources & evidence

ORD record
ord-bad212d73fbe4443a3779d8e411fab66
Source dataset
uspto-grants-2013_02
Patent number
US08378107B2

Reaction notes

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