3-Bromo-6-methylquinoline → HCID 71239222, compound

HRID 1424298Notes

Reaction equation

HRID 1424298 reaction equation
[CH3:1][CH:2]([CH3:31])[CH2:3][CH:4]([C:17]1[CH:30]=[CH:29][C:20]([C:21]([NH:23][CH2:24][CH2:25][C:26]([OH:28])=[O:27])=[O:22])=[CH:19][CH:18]=1)[NH:5][C:6]1[CH:7]=[N:8][C:9]2[C:14]([CH:15]=1)=[CH:13][CH:12]=[CH:11][C:10]=2C.Br[C:33]1C=NC2C(C=1)=CC(C)=CC=2>>[CH3:31][CH:2]([CH3:1])[CH2:3][CH:4]([C:17]1[CH:18]=[CH:19][C:20]([C:21]([NH:23][CH2:24][CH2:25][C:26]([OH:28])=[O:27])=[O:22])=[CH:29][CH:30]=1)[NH:5][C:6]1[CH:7]=[N:8][C:9]2[C:14]([CH:15]=1)=[CH:13][C:12]([CH3:33])=[CH:11][CH:10]=2

Participants

3

Reactant 2

HCID 124656203-Bromo-6-methylquinolineHCID 71239510HCID 71239510, compound

Product 1

HCID 71239222HCID 71239222, compound

Procedure

Prepared analogous to 3-{4-[3-Methyl-1-(8-methyl-quinolin-3-ylamino)-butyl]-benzoylamino}-propionic acid, Example 25, using 3-bromo-6-methylquinoline. m/z (M+1)=420.2.

Sources & evidence

ORD record
ord-39fd098f2fc34023abbef2547f665919
Source dataset
uspto-grants-2015_01
Patent number
US08927577B2

Reaction notes

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