4-Acetylbenzoic Acid → HCID 10194429, compound

HRID 10690Notes

Reaction equation

HRID 10690 reaction equation
[CH3:1][O:2][C:3]1[CH:10]=[C:9]([O:11][CH3:12])[C:8]([C:13]2[N:14]=[C:15]([CH3:18])[S:16][CH:17]=2)=[CH:7][C:4]=1[CH:5]=O.[C:19]([C:22]1[CH:30]=[CH:29][C:25]([C:26]([OH:28])=[O:27])=[CH:24][CH:23]=1)(=[O:21])[CH3:20]>>[CH3:1][O:2][C:3]1[CH:10]=[C:9]([O:11][CH3:12])[C:8]([C:13]2[N:14]=[C:15]([CH3:18])[S:16][CH:17]=2)=[CH:7][C:4]=1/[CH:5]=[CH:20]/[C:19]([C:22]1[CH:30]=[CH:29][C:25]([C:26]([OH:28])=[O:27])=[CH:24][CH:23]=1)=[O:21]

Participants

3

Reactant 2

HCID 114704-Acetylbenzoic AcidHCID 219811212,4-Dimethoxy-5-(2-methyl-thiazol-4-yl)-benzaldehyde

Product 1

HCID 10194429HCID 10194429, compound

Procedure

The title compound was prepared by condensing 2,4-dimethoxy-5-(2-methyl-thiazol-4-yl)-benzaldehyde (Ex-69A) and 4-acetylbenzoic acid in a similar manner as described in Ex-3. Yellow solid, mp 201–202° C. (dec.). 1H-NMR (DMSO-d6) δ 8.47 (s, 1H), 8.14–7.97 (m, 5H), 7.76 (s, 1H), 7.65 (d, J=15.8 Hz, 1H), 6.81 (s, 1H), 4.00 (s, 3H), 3.98 (s, 3H), 2.69 (s, 3H). MS m/z=409 (M+, 70%), 378 ([M−OCH3]+, 100%).

Sources & evidence

ORD record
ord-de02eab211fe46eb88ec524083dacd35
Source dataset
uspto-grants-2006_08
Patent number
US07094801B2

Reaction notes

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