4,7-Dichloroquinoline → HCID 10045028, compound

HRID 2354930Notes

Reaction equation

HRID 2354930 reaction equation
Cl[C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[N:7]([CH2:11][C:12]([OH:14])=[O:13])[C:6]([CH2:15]O)=[C:5]2[C:17]1[C:26]2[C:21](=[CH:22][C:23]([Cl:27])=[CH:24][CH:25]=2)[N:20]=[CH:19][CH:18]=1.ClC1C2C(=CC(Cl)=CC=2)[N:32]=[CH:31]C=1>>[Cl:27][C:23]1[CH:22]=[C:21]2[C:26]([C:17]([C:5]3[C:4]4[C:8](=[CH:9][CH:10]=[C:2]([C:31]#[N:32])[CH:3]=4)[N:7]([CH2:11][C:12]([OH:14])=[O:13])[C:6]=3[CH3:15])=[CH:18][CH:19]=[N:20]2)=[CH:25][CH:24]=1

Participants

3

Reactant 2

HCID 68664,7-DichloroquinolineHCID 10069607HCID 10069607, compound

Product 1

HCID 10045028HCID 10045028, compound

Procedure

The sub-title compound was prepared from the product of example 55, step a) and 4,7-dichloroquinoline by the method of example 55, step b).

Sources & evidence

ORD record
ord-1f271e9b690b427d894233964f7b7d15
Source dataset
uspto-grants-2010_07
Patent number
US07754735B2

Reaction notes

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