Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473975Generated: October 30, 2026

Acetonitrile → 2-(cis-2,6-Dimethyl-morpholin-4-yl)-thiazole-4-carbonitrile

https://huagongshe.com/reaction/473975

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantTriphenylphosphineHCID 11776—
Reactant4-(4-Bromo-thiazol-2-yl)-cis-2,6-dimethyl-morpholineHCID 67216896—
CatalystZinc cyanide (Zn(CN)2)HCID 11186—
CatalystHCID 178418397HCID 178418397—
Product2-(cis-2,6-Dimethyl-morpholin-4-yl)-thiazole-4-carbonitrileHCID 6721601760%

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of Intermediate 1 (52.8 g, 190.49 mmol), triphenylphosphine (4.99 g, 19.05 mmol), zinc cyanide (22.37 g, 190.49 mmol) and dry acetonitrile (360 mL) was introduced in a pressure tube and was degassed with nitrogen for 5 min. Tetrakis(triphenylphosphine)palladium (11 g, 9.52 mmol) was added and the mixture was further degassed for 5 min. The tube was sealed and the reaction mixture was stirred at 140° C. for 3 h. The suspension was evaporated and taken up in water/DCM. The combined organic layer was separated, filtered on a plug of diatomaceous earth, dried on MgSO4, filtered off, and evaporated. The residue was purified on an 800 g EasyVarioPrep (Merck) column (eluent: DCM). The desired fractions were concentrated in vacuo and dried in a vacuum oven at 50° C. overnight, yielding 25.6 g (60%) of Intermediate 2 as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637510B2
Source datasetuspto-grants-2014_01
ORD IDord-04197a26a77e45b48e48162075efe4ed
Source noteuspto-grants-2014_01