Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712102Generated: October 29, 2026

(2R)-2-hydroxypropanamide → HCID 86717556, compound

https://huagongshe.com/reaction/712102

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2R)-2-hydroxypropanamideHCID 1530236—
ReactantTriethyloxonium tetrafluoroborateHCID 2723982—
ReactantHCID 86717555HCID 86717555—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86717556HCID 8671755661.3%

Reaction Steps

A mixture of (2R)-2-hydroxypropanamide (17.1 mg, 0.192 mmol) and triethyloxonium tetrafluoroborate (34.2 mg, 0.180 mmol) in tetrahydrofuran (0.36 mL) was stirred at room temperature for 75 min and then concentrated. The residue was dissolved in ethanol (0.14 mL), and this solution was then added to a solution of benzyl [(1R,2R,5S)-5-[(6-aminothieno[3,2-b]pyridin-7-yl)amino]-2-(cyanomethyl)cyclohexyl]carbamate (26 mg, 0.060 mmol) in ethanol (0.36 mL) in a vial. The resulting mixture was stirred at 80° C. overnight. After cooling, the mixture was concentrated and purified on silica gel, eluted with 0-10% MeOH in dichloromethane to give 18 mg of the desired product. LCMS calculated for C26H28N5O3S (M+H)+: m/z=490.2. Found: 490.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181271B2
Source datasetuspto-grants-2015_11
ORD IDord-1270c9a921da49d68d4f25f1c384d2cf
Source noteuspto-grants-2015_11