1-Aminocyclopentanemethanol → HCID 10110783, compound

HRID 1831469Notes

Reaction equation

HRID 1831469 reaction equation
[C:1]1([CH2:7][S:8][C:9]2[N:10]=[C:11](Cl)[C:12]3[S:17][C:16]([NH2:18])=[N:15][C:13]=3[N:14]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[NH2:20][C:21]1([CH2:26][OH:27])[CH2:25][CH2:24][CH2:23][CH2:22]1>>[NH2:18][C:16]1[S:17][C:12]2[C:11]([NH:20][C:21]3([CH2:26][OH:27])[CH2:25][CH2:24][CH2:23][CH2:22]3)=[N:10][C:9]([S:8][CH2:7][C:1]3[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=3)=[N:14][C:13]=2[N:15]=1

Participants

3

Reactant 2

HCID 663071-AminocyclopentanemethanolHCID 112782745-(Benzylthio)-7-chloro[1,3]thiazolo[4,5-d]pyrimidin-2-amine

Product 1

HCID 10110783HCID 10110783, compound

Procedure

Prepared according to the procedure in Example 1, from 5-phenylmethylthio-7-chloro-thiazolo[4,5-d]pyrimidin-2-ylamine and cycloleucinol.

Workup

  1. customPrepared

Sources & evidence

ORD record
ord-16644bb6e56646d8ba98d427b441bd55
Source dataset
uspto-grants-2006_06
Patent number
US07067657B2

Reaction notes

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