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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 543777Generated: October 28, 2026

5-Bromopentanenitrile → HCID 20202803, compound

https://huagongshe.com/reaction/543777

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-BromopentanenitrileHCID 79435—
Reactant1,1,1-Trifluoro-2-isothiocyanatoethaneHCID 13883777—
ReactantHCID 20202779HCID 20202779—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
SolventAcetonitrileHCID 6342—
ProductHCID 20202803HCID 20202803—

Reaction Steps

To a solution of potassium t-butoxide (0.88 g.) in DMF (30 ml.) stirred at 0° under nitrogen was added 4-amino-2-phenylsulphinylmethylpyrimidine (1.84 g.). The solution was stirred for 10 minutes and 5-bromo-valeronitrile (1.3 g.) in DMF (5 ml.) added over 5 minutes. The mixture was stirred for 30 minutes at 0°, poured into water (150 ml.) and extracted with EtOAc (4×15 ml.) and the extract dried (MgSO4) and evaporated in vacuo to give a clear gum (1.7 g.). The gum was heated in toluene (40 ml.) at reflux for 30 minutes during which time it dissolved. The toluene was evaporated in vacuo and the residue partitioned between CH2Cl2 and 1 M aqueous hydrochloric acid. The aqueous layer was basified with 4 M aqueous sodium hydroxide and extracted with CH2Cl2 (3×15 ml.), the extract dried (MgSO4) and evaporated in vacuo to give a clear gum (900 mg.). To this gum (900 mg.) in acetonitrile (20 ml.) was added 2,2,2-trifluoroethylisothiocyanate (500 ml.) and the solution heated under reflux for 19 hours. The acetonitrile was evaporated in vacuo and trans-6-[4-(3-[2,2,2-trifluoroethyl]thioureido)pyrimid-2-yl]hex-5-enenitrile was isolated from the mixture by medium pressure chromatography on silica using EtOAc/cyclohexane 3:7 v/v as eluant.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04447441
Source datasetuspto-grants-1984_05
ORD IDord-856a2a650cd24baab3167bb911aced45
Source noteuspto-grants-1984_05