p-Aminophenylacetic acid ethyl ester → HCID 66913600, compound

HRID 2104532Notes

Reaction equation

HRID 2104532 reaction equation
[C:1]([C:9]1[CH:10]=[N:11][C:12]2[C:17]([C:18]=1[C:19]1[CH:20]=[C:21]([CH:24]=[CH:25][CH:26]=1)[CH:22]=O)=[CH:16][CH:15]=[CH:14][C:13]=2[C:27]([F:30])([F:29])[F:28])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C([O:33][C:34](=[O:43])[CH2:35][C:36]1[CH:41]=[CH:40][C:39]([NH2:42])=[CH:38][CH:37]=1)C>>[C:1]([C:9]1[CH:10]=[N:11][C:12]2[C:17]([C:18]=1[C:19]1[CH:20]=[C:21]([CH:24]=[CH:25][CH:26]=1)[CH2:22][NH:42][C:39]1[CH:38]=[CH:37][C:36]([CH2:35][C:34]([OH:33])=[O:43])=[CH:41][CH:40]=1)=[CH:16][CH:15]=[CH:14][C:13]=2[C:27]([F:30])([F:29])[F:28])(=[O:8])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

3

Reactant 2

HCID 225219p-Aminophenylacetic acid ethyl esterHCID 860556033-[3-Benzoyl-8-(trifluoromethyl)quinolin-4-yl]benzaldehyde

Product 1

HCID 66913600HCID 66913600, compound

Procedure

The title compound was prepared from 3-[3-benzoyl-8-(trifluoromethyl)quinolin-4-yl]benzaldehyde and (4-amino-phenyl)-acetic acid ethyl ester according to the procedure of Example 66. MS m/z 541.

Sources & evidence

ORD record
ord-933ce88e81f840309adfe50bb7d3065e
Source dataset
uspto-grants-2009_08
Patent number
US07576215B2

Reaction notes

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