Dichloromethane → 5-Bromopyrimidine-2-carbonitrile

HRID 1992549Notes

Reaction equation

HRID 1992549 reaction equation
[Br:1][C:2]1[CH:3]=[N:4][C:5](Cl)=[N:6][CH:7]=1.[C-]#N.[Na+].C1N2CC[N:14](CC2)[CH2:13]1.ClCCl>CS(C)=O.O>[Br:1][C:2]1[CH:3]=[N:4][C:5]([C:13]#[N:14])=[N:6][CH:7]=1

Participants

7

Procedure

A solution of 5-bromo-2-chloropyrimidine (10 g, 51.8 mmol) in dimethylsulfoxide (26 mL) was added to a mixture of sodium cyanide (2.59 g, 51.8 mmol) and triethylenediamine (1.2 g, 10.4 mmol) in dimethylsulfoxide (14 mL) and water (28 mL). The resulting mixture was stirred for 18 hours at room temperature. The mixture was then diluted with water (130 mL) and extracted with diethyl ether (3×150 mL). The combined organic solutions were dried over sodium sulfate and concentrated in vacuo to give a pale yellow solid. Re-crystallisation of the solid from hot dichloromethane afforded the title product in 99% yield, 9.4 g.

Workup

  1. extractionextracted with diethyl ether (3×150 mL)
  2. dry with materialThe combined organic solutions were dried over sodium sulfate
  3. concentrationconcentrated in vacuo
  4. customto give a pale yellow solid

Sources & evidence

ORD record
ord-718ce3fd31ec4996b881ab5032c2ea78
Source dataset
uspto-grants-2010_01
Patent number
US07649003B2

Reaction notes

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