Water → HCID 13008377, compound
Reaction equation
[Br:1][C:2]1[C:6]([N+:7]([O-:9])=[O:8])=[C:5](Br)[N:4]([CH2:11][C:12]2[CH:17]=[CH:16][CH:15]=[C:14]([CH2:18][N:19]3[C:23](Br)=[C:22]([N+:25]([O-:27])=[O:26])[C:21]([Br:28])=[N:20]3)[CH:13]=2)[N:3]=1.[CH2:29]([NH2:36])[C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1.O>C(O)CC>[CH2:29]([NH:36][C:23]1[N:19]([CH2:18][C:14]2[CH:15]=[CH:16][CH:17]=[C:12]([CH2:11][N:4]3[C:5]([NH:4][CH2:11][C:12]4[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=4)=[C:6]([N+:7]([O-:9])=[O:8])[C:2]([Br:1])=[N:3]3)[CH:13]=2)[N:20]=[C:21]([Br:28])[C:22]=1[N+:25]([O-:27])=[O:26])[C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
13.9 g of 1,3-bis-(3,5-dibromo-4-nitropyrazol-1-yl-methyl)benzene from step 4.1 are heated together with 6.5 g of benzylamine in 130 ml of n-propanol for 2 hours at 95° C. Subsequently the reaction mixture is cooled and poured into 400 ml water. The precipitate is filtered with suction and recyrstallized from 150 ml of acetonitrile.
Workup
- temperatureSubsequently the reaction mixture is cooled
- filtrationThe precipitate is filtered with suction
Sources & evidence
- ORD record
- ord-8567ba65e8ac4b1a8c6665cbe6cf0963
- Source dataset
- uspto-grants-2004_04
- Patent number
- US06716257B2
Reaction notes
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