Isatoic Anhydride → HCID 22493278, compound
Reaction equation
[NH2:1][C:2]1[CH:15]=[CH:14][CH:13]=[CH:12][C:3]=1[C:4]([N:6]([CH2:8][CH2:9][O:10][CH3:11])[CH3:7])=[O:5].COC[CH2:19][NH:20]C.C12[C:28](=[CH:29]C=CC=1)[NH:27][C:26](=O)OC2=O>>[NH:27]1[CH2:26][CH2:19][N:20]=[C:28]1[CH2:29][NH:1][C:2]1[CH:15]=[CH:14][CH:13]=[CH:12][C:3]=1[C:4]([N:6]([CH2:8][CH2:9][O:10][CH3:11])[CH3:7])=[O:5]Participants
4
Procedure
2-Amino-N-(2-methoxyethyl)-N-methylbenzamide (prepared from N-(2-methoxyethyl)methylamine and isatoic anhydride, using the methods described in Example 17) and CMI were reacted using conditions described in the general procedure for CMI coupling to give 2-[(4,5-dihydro-1H-imidazol-2-ylmethyl)amino]-N-(2-methoxyethyl)-N-methylbenzamide.
Workup
- customwere reacted
Sources & evidence
- ORD record
- ord-53d869e1b41048449905707504f0a613
- Source dataset
- uspto-grants-2005_04
- Patent number
- US06884801B1
Reaction notes
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