Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 921725Generated: October 31, 2026

(2S)-2-Methyloxirane → HCID 86708606, compound

https://huagongshe.com/reaction/921725

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2S)-2-MethyloxiraneHCID 146262—
ReactantHCID 86708607HCID 86708607—
SolventMethanolHCID 887—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 86708606HCID 8670860632.9%

Reaction Conditions

Temperature50 °C

Reaction Steps

A suspension of 2-((3-(azetidin-3-yl)-2-chloro-5-cyanophenyl)amino)-4-(ethylamino)imidazo[2,1-f][1,2,4]triazine-7-carbonitrile (Example 367)(16 mg, 0.041 mmol) and (S)-(−)-propylene oxide (0.085 mL, 1.22 mmol) in a mixture of NMP (0.8 mL) and MeOH (0.2 mL) was stirred at 50° C. for 4.5 hr. The solvent was removed and the product was purified by preparative HPLC (Waters XBridge C18, 19×200 mm, 5-μm particles; Mobile Phase A: water with 20-mM ammonium acetate; Mobile Phase B: 95:5 acetonitrile: water with 20-mM ammonium acetate; Gradient: 15-55% B over 20 minutes, then a 5-minute hold at 100% B; Flow: 20 mL/min) to give the title compound (6.1 mg). This was converted to the mono HCl salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273057B2
Source datasetuspto-grants-2016_03
ORD IDord-ca3cf582faa04b27bafb7bf512a1fadf
Source noteuspto-grants-2016_03