Triethylamine → HCID 22099546, compound
Reaction equation
[N:1]1[C:6]2[NH:7][C:8]3[CH:15]=[CH:14][CH:13]=[CH:12][C:9]=3[CH2:10][NH:11][C:5]=2[CH:4]=[CH:3][CH:2]=1.[F:16][C:17]1[CH:18]=[CH:19][C:20]([CH3:35])=[C:21]([CH:34]=1)[C:22]([NH:24][C:25]1[N:30]=[CH:29][C:28]([C:31](Cl)=[O:32])=[CH:27][CH:26]=1)=[O:23].C(N(CC)CC)C>ClCCl>[N:1]1[C:6]2[NH:7][C:8]3[CH:15]=[CH:14][CH:13]=[CH:12][C:9]=3[CH2:10][N:11]([C:31]([C:28]3[CH:27]=[CH:26][C:25]([NH:24][C:22](=[O:23])[C:21]4[CH:34]=[C:17]([F:16])[CH:18]=[CH:19][C:20]=4[CH3:35])=[N:30][CH:29]=3)=[O:32])[C:5]=2[CH:4]=[CH:3][CH:2]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
As described for Example 1, 6,11-dihydro-5H-pyrido[2,3-b][1,4]benzodiazepine (2 mmol) is reacted with 6-[(5-fluoro-2-methylbenzoyl)amino]pyridine-3-carbonyl chloride (2.1 mmol) in the presence of triethylamine (4 mmol) in dichloromethane to give the product as a solid, m.p. 102° C.-104° C.
Sources & evidence
- ORD record
- ord-22a951f5b7e443d7a678962dbb01a0dd
- Source dataset
- uspto-grants-1998_12
- Patent number
- US05849735
Reaction notes
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