HCID 21702781, compound → HCID 58306151, compound

HRID 1044860Notes

Reaction equation

HRID 1044860 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][CH:16]2[CH2:21][CH2:20]N(CC)CC2)=[C:8]([NH2:26])[N:7]=1)[CH2:2][CH2:3][CH3:4].C(OC1NC(N)=C2C(N=1)=NC(OC)=N2)CCC.[CH2:44]([N:46]1[CH2:51]CC(CCO)[CH2:48][CH2:47]1)[CH3:45]>>[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][CH:21]2[CH2:20][CH2:51][N:46]([CH2:47][CH3:48])[CH2:44][CH2:45]2)=[C:8]([NH2:26])[N:7]=1)[CH2:2][CH2:3][CH3:4]

Participants

4

Procedure

Prepared similarly to Intermediate 19 from 2-(butyloxy)-8-(methyloxy)-1H-purin-6-amine and 2-(1-ethyl-4-piperidinyl)ethanol.

Sources & evidence

ORD record
ord-8a9689365acc4cabb2d474f263d9ab97
Source dataset
uspto-grants-2013_10
Patent number
US08563717B2

Reaction notes

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