Benzyl Alcohol → HCID 13371681, compound

HRID 638181Notes

Reaction equation

HRID 638181 reaction equation
Cl[C:2]1[N:3]=[C:4]2[C:9](=[N:10][C:11]=1[N:12]([CH3:14])[CH3:13])[N:8]=[C:7]([N:15]1[CH2:20][CH2:19][NH:18][CH2:17][CH2:16]1)[N:6]=[C:5]2[N:21]([CH3:23])[CH3:22].[CH2:24]([OH:31])[C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1>>[CH2:24]([O:31][C:2]1[N:3]=[C:4]2[C:9](=[N:10][C:11]=1[N:12]([CH3:14])[CH3:13])[N:8]=[C:7]([N:15]1[CH2:20][CH2:19][NH:18][CH2:17][CH2:16]1)[N:6]=[C:5]2[N:21]([CH3:23])[CH3:22])[C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1

Participants

3

Reactant 2

HCID 244Benzyl AlcoholHCID 30246534,7-Pteridinediamine, 6-chloro-N,N,N',N'-tetramethyl-2-(1-piperazinyl)-

Product 1

HCID 13371681HCID 13371681, compound

Procedure

This compound was prepared analogous to Example 3 from 6-chloro-4,7-bis-(dimethylamino)-2-piperazino-pteridine and benzyl alcohol.

Sources & evidence

ORD record
ord-92a835a62664425585873eb894ec47d6
Source dataset
uspto-grants-1985_12
Patent number
US04560685

Reaction notes

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