(Oxolan-3-yl)methanamine hydrochloride → HCID 67224141, compound
Reaction equation
[CH2:1]([O:5][C:6]1[N:14]=[C:13]2[C:9]([N:10]=[C:11]([O:24][CH3:25])[N:12]2[CH2:15][CH2:16][CH2:17][NH:18][C@@H:19]2[CH2:23][CH2:22][CH2:21][O:20]2)=[C:8]([NH2:26])[N:7]=1)[CH2:2][CH2:3][CH3:4].F[C:28](F)(F)C(O)=O.C(OC1NC(N)=C2C(N=1)=NC(OC)=N2)CCC.Cl.O1CCC(CN)C1>>[CH2:1]([O:5][C:6]1[N:14]=[C:13]2[C:9]([N:10]=[C:11]([O:24][CH3:25])[N:12]2[CH2:15][CH2:16][CH2:17][NH:18][CH2:19][CH:23]2[CH2:22][CH2:21][O:20][CH2:28]2)=[C:8]([NH2:26])[N:7]=1)[CH2:2][CH2:3][CH3:4]Participants
4
Procedure
Prepared similarly to Intermediate 14 from 2-(butyloxy)-8-(methyloxy)-1H-purin-6-amine trifluoroacetate and (tetrahydro-3-furanylmethyl)amine hydrochloride.
Sources & evidence
- ORD record
- ord-1a17005db2374f0298009f087d6edd35
- Source dataset
- uspto-grants-2013_11
- Patent number
- US08575181B2
Reaction notes
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