Triethylamine → Cyclopropanecarboxylic Acid 2-methyl-4-(2-methyl-4,5-dihydro-1-oxa-3,6-diaza-benzo[e]azulene-6-carbonyl)-benzylamide
Reaction equation
[CH:1]1([C:4](Cl)=[O:5])[CH2:3][CH2:2]1.Cl.[NH2:8][CH2:9][C:10]1[CH:15]=[CH:14][C:13]([C:16]([N:18]2[CH2:27][CH2:26][C:25]3[N:24]=[C:23]([CH3:28])[O:22][C:21]=3[C:20]3[CH:29]=[CH:30][CH:31]=[CH:32][C:19]2=3)=[O:17])=[CH:12][C:11]=1[CH3:33].C(N(CC)CC)C>ClCCl>[CH3:33][C:11]1[CH:12]=[C:13]([C:16]([N:18]2[CH2:27][CH2:26][C:25]3[N:24]=[C:23]([CH3:28])[O:22][C:21]=3[C:20]3[CH:29]=[CH:30][CH:31]=[CH:32][C:19]2=3)=[O:17])[CH:14]=[CH:15][C:10]=1[CH2:9][NH:8][C:4]([CH:1]1[CH2:3][CH2:2]1)=[O:5]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Cyclopropanecarbonyl chloride (26 mg, 0.25 mmol) was added to a solution of (4-aminomethyl-3-methyl-phenyl)-(2-methyl-4,5-dihydro-1-oxa-3,6-diaza-benzo[e]azulen-6-yl)-methanone hydrochloride from Example E119.2 (85 mg, 0.22 mmol) in dichloromethane (5 ml) and triethylamine (to pH9) at room temperature. The mixture was stirred for 1 h then purified by flash chromatography on silica gel (eluant; 10% methanol:90% dichloromethane) to give a white solid identified as the title compound (62 mg, 67%).
Workup
- customat room temperature
- customthen purified by flash chromatography on silica gel (eluant; 10% methanol:90% dichloromethane)
- customto give a white solid
Sources & evidence
- ORD record
- ord-a29c0c6d62334a61862b17a89e07f14f
- Source dataset
- uspto-grants-2012_06
- Patent number
- US08202858B2
Reaction notes
Loading…