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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712061Generated: October 30, 2026

Triethyl orthoacetate → HCID 86717521, compound

https://huagongshe.com/reaction/712061

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethyl orthoacetateHCID 66221—
ReactantHCID 86717520HCID 86717520—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 86717521HCID 8671752142.2%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of {(2R,5S)-5-[(6-aminothieno[3,2-b]pyridin-7-yl)amino]tetrahydro-2H-pyran-2-yl}methanol (131 mg, 0.469 mmol) in acetic acid (1.3 mL) was added triethyl orthoacetate (275 μL, 1.50 mmol). The mixture was stirred at 120° C. for 30 min. After cooling to room temperature, the mixture was diluted with methanol and purified with prep-LCMS (XBridge C18 column, eluting with a gradient of acetonitrile/water containing 0.1% ammonium hydroxide, at flow rate of 60 mL/min) to give the desired product as white solid (60 mg, 42%). LCMS calculated for C15H18N3O2S (M+H)+: m/z=304.1. Found: 304.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181271B2
Source datasetuspto-grants-2015_11
ORD IDord-cad1f3e272e2418283d1f93e80d9625b
Source noteuspto-grants-2015_11