Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243543Generated: October 25, 2026

Acetonitrile → Etravirine

https://huagongshe.com/reaction/243543

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantN-[5-bromo-6-(4-cyano-2,6-dimethylphenoxy)-2-(4-cyano-phenylamino)pyrimidin-4-yl]benzamideHCID 70978955—
SolventIsopropanolHCID 3776—
ProductEtravirineHCID 193962—

Reaction Conditions

Temperature59 °C

Reaction Steps

1350 ml of acetonitrile was taken into a RB flask at 27±3° C. To this was added 900 ml of IPA. To the reaction mixture 150 g of N-[5-bromo-6-(4-cyano-2,6-dimethylphenoxy)-2-(4-cyano-phenylamino)pyrimidin-4-yl]benzamide and 35.2 g of lithium hydroxide monohydrate were added and heated to 59±3° C. The reaction mixture was maintained at the same temperature for 10 hrs. After completion of the reaction, the reaction mixture was cooled to 47±3° C. and filtered. The solid was washed with acetonitrile and suck dried. The wet cake was taken into another flask to which was added 1500 ml of water, stirred for 30 mins and filtered to obtain the solid. The solid was washed with water and dried under vacuum at 73±3° C. to isolate Etravirine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653266B2
Source datasetuspto-grants-2014_02
ORD IDord-91e5b7c5f356461e878247d8e5899502
Source noteuspto-grants-2014_02