Hydrochloric Acid → HCID 178455636, compound
Reaction equation
[C:1]1([CH:7]([C:34]2[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=2)[CH2:8][NH:9][C:10]2[N:18]=[C:17]([CH2:19][NH:20][S:21]([CH2:24][CH:25]([CH3:27])[CH3:26])(=[O:23])=[O:22])[N:16]=[C:15]3[C:11]=2[N:12]=[CH:13][N:14]3C2CCCCO2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[ClH:40]>C(O)C>[ClH:40].[C:34]1([CH:7]([C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)[CH2:8][NH:9][C:10]2[N:18]=[C:17]([CH2:19][NH:20][S:21]([CH2:24][CH:25]([CH3:27])[CH3:26])(=[O:22])=[O:23])[N:16]=[C:15]3[C:11]=2[N:12]=[CH:13][NH:14]3)[CH:35]=[CH:36][CH:37]=[CH:38][CH:39]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of N-({6-[(2,2-diphenylethyl)amino]-9-tetrahydro-2H-pyran-2-yl-9H-purin-2-yl}methyl)-2-methyl-1-propanesulfonamide (4.30 g, 7.84 mmol) (Preparation 7) in ethanol (100 ml) was heated to 37° C. and then treated with hydrochloric acid (2N, 15 ml). The mixture was left to stand at room temperature for 18 hours, after which time a crystalline precipitate was filtered off, washed with ethanol (10 ml) and dried to afford the title compound as a solid (3.0 g).
Workup
- waitThe mixture was left
- filtrationafter which time a crystalline precipitate was filtered off
- washwashed with ethanol (10 ml)
- customdried
Sources & evidence
- ORD record
- ord-91a9ee6edaf44aa79061155e2704801d
- Source dataset
- uspto-grants-2002_02
- Patent number
- US06350735B1
Reaction notes
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