2-Amino-5-methoxybenzamide → HCID 178487727, compound

HRID 643846Notes

Reaction equation

HRID 643846 reaction equation
NC1C=CC(OC)=CC=1[C:4](N)=[O:5].[C:13]1([C:19]2[N:28]=[C:27]([OH:29])[C:26]3[C:21](=[CH:22][CH:23]=[CH:24][CH:25]=3)[N:20]=2)[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>>[CH3:4][O:5][C:23]1[CH:22]=[C:21]2[C:26]([C:27]([OH:29])=[N:28][C:19]([C:13]3[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=3)=[N:20]2)=[CH:25][CH:24]=1

Participants

3

Reactant 2

HCID 203382172-Amino-5-methoxybenzamideHCID 178517457HCID 178517457, compound

Product 1

HCID 178487727HCID 178487727, compound

Procedure

Treatment of 2-amino-5-methoxy-benzamide according the procedure described by Raid J. Abdel-Jalil, Wolfgang Voelter and Muhammad Saeed in Tetrahedron Letters 45 (2004) 3475-3476 for the preparation of 2-phenyl-quinazoline 4-ol gave the title compound.

Sources & evidence

ORD record
ord-34d593f0266044a1a3dca8700c4ca9b3
Source dataset
uspto-grants-2010_04
Patent number
US07700552B2

Reaction notes

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