4-Acetylbenzoic Acid → 4-[3E-(2-Pyrrolidin-1-yl-5-thiophen-2-yl-phenyl)-acryloyl]-benzoic acid

HRID 10684ノート

反応式

HRID 10684 の反応式
[N:1]1([C:6]2[CH:13]=[CH:12][C:11]([C:14]3[S:15][CH:16]=[CH:17][CH:18]=3)=[CH:10][C:7]=2[CH:8]=O)[CH2:5][CH2:4][CH2:3][CH2:2]1.[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]>>[N:1]1([C:6]2[CH:13]=[CH:12][C:11]([C:14]3[S:15][CH:16]=[CH:17][CH:18]=3)=[CH:10][C:7]=2/[CH:8]=[CH:20]/[C:19]([C:22]2[CH:30]=[CH:29][C:25]([C:26]([OH:28])=[O:27])=[CH:24][CH:23]=2)=[O:21])[CH2:5][CH2:4][CH2:3][CH2:2]1

参加物

3

反応物 2

HCID 114704-Acetylbenzoic AcidHCID 219810662-Pyrrolidin-1-yl-5-thiophen-2-yl-benzaldehyde

生成物 1

HCID 103097294-[3E-(2-Pyrrolidin-1-yl-5-thiophen-2-yl-phenyl)-acryloyl]-benzoic acid

実験手順

The title compound was prepared by condensing 2-pyrrolidin-1-yl-5-thiophen-2-yl-benzaldehyde (Ex-63A) and 4-acetylbenzoic acid in a similar manner as described in Ex-3. Red solid, mp 208–209° C. 1H-NMR (DMSO-d6) δ 12.50 (bs, 1H), 8.22 (d, J=8.5 Hz, 2H), 8.09–7.99 (m, 4H), 7.73 (d, J=15.5 Hz, 1H), 7.52–7.41 (m, 3H), 7.10–7.07 (m, 1H), 6.93 (d, J=9.0 Hz, 1H), 3.28 (m, 4H), 1.87 (m, 4H).

出典と根拠

ORDレコード
ord-7dbd754bf91c4bb18f0bbef2763fd3b3
出典データセット
uspto-grants-2006_08
特許番号
US07094801B2

反応ノート

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