Triethylamine → HCID 86752394, compound
Reaction equation
NC1[CH:24]=[CH:23][C:5]([C:6]([N:8]2[CH2:14][C:13]3[CH:15]=[CH:16][CH:17]=[CH:18][C:12]=3[CH2:11][C:10]3[CH:19]=[CH:20][CH:21]=[CH:22][C:9]2=3)=[O:7])=[CH:4]C=1.CC1C=C[S:28][C:27]=1[C:31](Cl)=[O:32].C([N:36](CC)CC)C>ClCCl>[CH:19]1[C:10]2[CH2:11][C:12]3[CH:18]=[CH:17][CH:16]=[CH:15][C:13]=3[CH2:14][N:8]([C:6]([C:5]3[C:23]([CH3:24])=[C:27]([C:31]([NH2:36])=[O:32])[S:28][CH:4]=3)=[O:7])[C:9]=2[CH:22]=[CH:21][CH:20]=1Participants
5
Procedure
As described for Example 9, 0.314 g (1 mmol) of 5-(4-aminobenzoyl)-6,11-dihydro-5H-dibenz[b,e]azepine is reacted with 0.177 g (1.1 mmol) of 3-methyl-2-thiophenecarbonyl chloride in 5 ml of dichloromethane and 0.111 g of triethylamine for 2 hours at room temperature to give crystals. Recrystallization from dichloromethane-hexane gives 0.235 g of crystals, m.p. 201°-204° C.
Workup
- customto give crystals
- customRecrystallization from dichloromethane-hexane
Sources & evidence
- ORD record
- ord-62b8f48f4b4d49ad91b51b16d260a476
- Source dataset
- uspto-grants-1998_04
- Patent number
- US05739128
Reaction notes
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