Quinoline-3-carboxylic acid → HCID 68838551, compound

HRID 1727269Notes

Reaction equation

HRID 1727269 reaction equation
[CH2:1]([O:3][C:4](=[O:36])[CH:5]=[CH:6][C:7]1[CH:12]=[CH:11][C:10]([CH2:13][NH:14][C:15](=[O:35])[C:16]2[CH:21]=[CH:20][C:19]([N:22]3[CH2:27]CN(CC4C=NC=CC=4)CC3)=[CH:18][CH:17]=2)=[CH:9][CH:8]=1)[CH3:2].N1C2C(=CC=CC=2)C=[C:39](C(O)=O)[CH:38]=1>>[CH2:1]([O:3][C:4](=[O:36])[CH:5]=[CH:6][C:7]1[CH:8]=[CH:9][C:10]([CH2:13][NH:14][C:15]([C:16]2[CH:27]=[N:22][C:19]3[C:20]([CH:21]=2)=[CH:39][CH:38]=[CH:17][CH:18]=3)=[O:35])=[CH:11][CH:12]=1)[CH3:2]

Participants

3

Reactant 2

HCID 80971Quinoline-3-carboxylic acidHCID 68841846HCID 68841846, compound

Product 1

HCID 68838551HCID 68838551, compoundYield 89%

Procedure

The titled compound was prepared as described in the process (1-2) by using 3-quinolinecarboxylic acid.

Sources & evidence

ORD record
ord-044a4c04f1474b3b8be9cf3387298898
Source dataset
uspto-grants-2009_02
Patent number
US07495022B2

Reaction notes

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