HCID 86608383, compound → HCID 68517032, compound

HRID 882751Notes

Reaction equation

HRID 882751 reaction equation
[N:1]([C:4]1[N:9]=[C:8]([N:10]2[CH2:15][CH2:14][O:13][CH2:12][CH2:11]2)[N:7]=[C:6]([O:16][CH2:17][C:18]([CH3:21])([OH:20])[CH3:19])[CH:5]=1)=[N+]=[N-]>O1CCCC1.CO.[Pd]>[NH2:1][C:4]1[N:9]=[C:8]([N:10]2[CH2:15][CH2:14][O:13][CH2:12][CH2:11]2)[N:7]=[C:6]([O:16][CH2:17][C:18]([CH3:21])([OH:20])[CH3:19])[CH:5]=1

Participants

5

Reactant 1

HCID 86608383HCID 86608383, compound

Product 1

HCID 68517032HCID 68517032, compound

Reagents, catalysts & solvents 3

HCID 23938PalladiumCatalystHCID 887MethanolSolventHCID 8028TetrahydrofuranSolvent

Procedure

1-(6-azido-2-morpholin-4-yl-pyrimidin-4-yloxy)-2-methyl-propan-2-ol was dissolved in a mixture of tetrahydrofuran (200 mL) and methanol (20 mL). To the solution was added 10% palladium on carbon (2 g) and the reaction was stirred under an atmosphere of hydrogen for 24 hours. The reaction was then filtered through celite and evaporated to give 1-(6-amino-2-morpholin-4-yl-pyrimidin-4-yloxy)-2-methyl-propan-2-ol (2.0 g).

Workup

  1. filtrationThe reaction was then filtered through celite
  2. customevaporated

Sources & evidence

ORD record
ord-47955d7c1dd74d03be43f5c92e5c30e1
Source dataset
uspto-grants-2012_08
Patent number
US08236795B2

Reaction notes

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