Tert-Butylamine → HCID 18789027, compound
Reaction equation
Cl[CH2:2][CH2:3][C:4]1[C:5]([Cl:14])=[N:6][C:7]2[N:8]([N:11]=[CH:12][CH:13]=2)[C:9]=1Cl.[C:15]([NH2:19])([CH3:18])([CH3:17])[CH3:16].C(N(CC)CC)C>CN(C)C=O>[C:15]([N:19]1[C:9]2[N:8]3[N:11]=[CH:12][CH:13]=[C:7]3[N:6]=[C:5]([Cl:14])[C:4]=2[CH2:3][CH2:2]1)([CH3:18])([CH3:17])[CH3:16]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
In 70 ml of dimethylformamide were dissolved 12.50 g of 6-(2-chloroethyl)-5,7-dichloropyrazolo[1,5-a]pyrimidine, and 9.55 g of tert-butylamine and 11.47 g of triethylamine were added to the solution. The mixture was stirred for 2 days at room temperature. Excess amines and the solvent were distilled off under reduced pressure, and the residue was dissolved in chloroform. After the chloroform layer was washed with a saturated saline solution and dried over anhydrous sodium sulfate, the solvent was distilled off. The residue was treated with a chloroform-ether system to deposit crystals. The crystals were collected by filtration and recrystallized from ethanol to obtain 11.34 g (yield: 90.6%) of the intended product.
Workup
- additionwere added to the solution
- distillationExcess amines and the solvent were distilled off under reduced pressure
- dissolutionthe residue was dissolved in chloroform
- washAfter the chloroform layer was washed with a saturated saline solution
- dry with materialdried over anhydrous sodium sulfate
- distillationthe solvent was distilled off
- additionThe residue was treated with a chloroform-ether system
- filtrationThe crystals were collected by filtration
- customrecrystallized from ethanol
Sources & evidence
- ORD record
- ord-7b7e2cb63d0d42e2bd576fe6b19ee07d
- Source dataset
- uspto-grants-2000_05
- Patent number
- US06057330
Reaction notes
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