HCID 86626004, compound → 952678-28-3

HRID 1712908Notes

Reaction equation

HRID 1712908 reaction equation
CS(O[CH2:6][CH2:7][O:8][CH:9]([C:15]1[CH:20]=[CH:19][C:18]([C:21]#[N:22])=[CH:17][CH:16]=1)[C:10]1[NH:11][CH:12]=[N:13][CH:14]=1)(=O)=O>C(#N)C>[CH:14]1[N:13]=[CH:12][N:11]2[CH2:6][CH2:7][O:8][CH:9]([C:15]3[CH:20]=[CH:19][C:18]([C:21]#[N:22])=[CH:17][CH:16]=3)[C:10]=12

Participants

3

Reactant 1

HCID 86626004HCID 86626004, compound

Product 1

HCID 23651251952678-28-3

Reagents, catalysts & solvents 1

HCID 6342AcetonitrileSolvent

Procedure

A solution of 1.20 mmol of 2-[(4-cyanophenyl)-(3H-imidazol-4-yl)methoxy]ethyl methanesulphonate in 10 ml of acetonitrile is heated to reflux for 24 hours. The reaction mixture is cooled to room temperature and evaporated. The title compound is obtained as a white solid from the residue by flash chromatography (SiO2 60F). Rf=0.14 (dichloromethane -2M ammonia in ethanol 95:5); Rt=4.29.

Workup

  1. temperatureto reflux for 24 hours
  2. customevaporated

Sources & evidence

ORD record
ord-efbaa6e3a15d401294c9915aa4bef7a2
Source dataset
uspto-grants-2010_09
Patent number
US07795253B2

Reaction notes

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