Nonanoic Acid → HCID 19027813, compound

HRID 2379625Notes

Reaction equation

[C:1]([OH:11])(=O)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH3:9].[CH2:12](Br)[CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18].[NH2:20][C:21]1[C:30]([S:31][CH3:32])=[CH:29][CH:28]=[C:27]2[C:22]=1[CH:23]=[CH:24][CH:25]=[N:26]2>>[CH3:32][S:31][C:30]1[C:21]([NH:20][C:1](=[O:11])[CH:2]([CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH3:9])[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18])=[C:22]2[C:27](=[CH:28][CH:29]=1)[N:26]=[CH:25][CH:24]=[CH:23]2

Participants

Reactant 3

HCID 8158Nonanoic Acid

HCID 123691-Bromoheptane

HCID 103976605-Amino-6-methylthioquinoline

Product 1

HCID 19027813HCID 19027813, compound

Procedure

By use of the procedures described in Example 25, nonanoic acid was alkylated with heptyl bromide and the resulting product was coupled with 5-amino-6-methylthioquinoline (Example 34) to give the title compound.

Sources & evidence

ORD record: ord-e793ab61006a4c4c8e8341c94859af4f
Source dataset: uspto-grants-1994_11
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05362878

Reaction notes

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