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Morpholine → 4-(5-Chlorothiazolo[4,5-d]pyrimidin-7-yl)morpholine

HRID 1408461
Notes
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Reaction equation

HRID 1408461 reaction equation
[Cl:1][C:2]1[N:3]=[C:4](Cl)[C:5]2[S:10][CH:9]=[N:8][C:6]=2[N:7]=1.[NH:12]1[CH2:17][CH2:16][O:15][CH2:14][CH2:13]1>CO>[Cl:1][C:2]1[N:3]=[C:4]([N:12]2[CH2:17][CH2:16][O:15][CH2:14][CH2:13]2)[C:5]2[S:10][CH:9]=[N:8][C:6]=2[N:7]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 8083MorpholineHCID 569495425,7-Dichlorothiazolo[4,5-d]pyrimidine

Product 1

HCID 576854144-(5-Chlorothiazolo[4,5-d]pyrimidin-7-yl)morpholineYield 100%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

A mixture of 5,7-dichlorothiazolo[4,5-d]pyrimidine (1.0 eq.), morpholine (2.2 eq.) and MeOH was stirred at room temperature for 1 h. The reaction mixture was then filtered, washed with water and MeOH, to yield 4-(5-chlorothiazolo[4,5-d]pyrimidin-7-yl)morpholine as a white solid (100%).

Workup

  1. filtrationThe reaction mixture was then filtered
  2. washwashed with water and MeOH

Sources & evidence

ORD record
ord-adcd960ccfb246bf94ef778be6da7fbe
Source dataset
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08921361B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes