Isopropylamine → HCID 20350130, compound
Reaction equation
Cl[C:2]1[N:10]=[CH:9][N:8]=[C:7]2[C:3]=1[N:4]=[CH:5][N:6]2[CH2:11][C:12]1[C:17]([Cl:18])=[CH:16][CH:15]=[CH:14][C:13]=1[Cl:19].[CH:20]([NH2:23])([CH3:22])[CH3:21]>CO>[Cl:19][C:13]1[CH:14]=[CH:15][CH:16]=[C:17]([Cl:18])[C:12]=1[CH2:11][N:6]1[CH:5]=[N:4][C:3]2[C:7]1=[N:8][CH:9]=[N:10][C:2]=2[NH:23][CH:20]([CH3:22])[CH3:21]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
6-Chloro-9-(2,6-dichlorobenzyl)purine (314 mg), 296 mg of isopropylamine and 25 ml of methanol were treated in the same manner as Example 2 and recrystallized from aqueous ethanol to obtain 276 mg (yield 79%) of 9-(2,6-dichlorobenzyl)-6-isopropylaminopurine as colorless needles melting at 109°-110° C.
Workup
- customrecrystallized from aqueous ethanol
Sources & evidence
- ORD record
- ord-c5ac9e87561e40ad98ee5393028f66e7
- Source dataset
- uspto-grants-1980_02
- Patent number
- US04189485
Reaction notes
Loading…