Ethylamine → N-Ethyl-6-methyl-2-(methylsulfanyl)pyrimidin-4-amine

HRID 1893879Notes

Reaction equation

HRID 1893879 reaction equation
Cl[C:2]1[CH:7]=[C:6]([CH3:8])[N:5]=[C:4]([S:9][CH3:10])[N:3]=1.[CH2:11]([NH2:13])[CH3:12]>O>[CH2:11]([NH:13][C:2]1[CH:7]=[C:6]([CH3:8])[N:5]=[C:4]([S:9][CH3:10])[N:3]=1)[CH3:12]

Participants

4

Conditions

Temperature
50 °C

Procedure

To the 4-chloro-6-methyl-2-(methylthio)pyrimidine from above was added 30 mL of a solution of 70% ethylamine in water. The reaction mixture was heated to 50° C. for 3 h. After completion, excess ethylamine was evaporated on rotary evaporator under vacuum. The solid was filtered and dried under vacuum to afford N-ethyl-6-methyl-2-(methylthio)pyrimidin-4-amine (20 g, 90% yield).

Workup

  1. customAfter completion, excess ethylamine was evaporated on rotary evaporator under vacuum
  2. filtrationThe solid was filtered
  3. customdried under vacuum

Sources & evidence

ORD record
ord-da795f83080b47748b44e9a35a6e67b8
Source dataset
uspto-grants-2013_08
Patent number
US08513266B2

Reaction notes

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