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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2353837Generated: November 1, 2026

Triethylamine → HCID 59380395, compound

https://huagongshe.com/reaction/2353837

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant(+)-GlycidolHCID 5460455—
ReactantHCID 59380394HCID 59380394—
SolventEthanolHCID 702—
ProductHCID 59380395HCID 5938039541.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 4-({3-chloro-4-[(3-fluorobenzyl)oxy]phenyl}amino)[1]benzothieno[2,3-d]pyrimidin-7-ol (30 mg, 0.07 mmol) in EtOH (1.0 mL) was added (R)-(+)-glycidol (5 mg, 0.07 mL, 1.0 equiv) and triethylamine (0.34 mg, 0.0035 mmol, 0.05 equiv) under nitrogen. The reaction mixture was stirred at 80° C. for 15 h and then cooled to rt. The solvents were removed in vacuo. The residue was purified by preparative HPLC to afford (2R)-3-{[4-({3-chloro-4-[(3-fluorobenzyl)oxy]phenyl}amino)[1]benzothieno[2,3-d]pyrimidin-7-yl]oxy}propane-1,2-diol as a white solid (14.8 mg, 40%). 1H-NMR (CD3OD) δ 8.45 (s, 1H), 8.32 (d, J=8.9 Hz, 1H), 7.73 (d, J=2.7 Hz, 1H), 7.61 (d, J=2.2 Hz, 1H), 7.46 (dd, J=2.7, 9.0 Hz, 1H), 7.40 (m, 1H), 7.30 (d, J=7.8 Hz, 1H), 7.25 (dd, J=2.3, 9.0 Hz, 2H), 7.16 (d, J=9 Hz, 1H), 7.05 (td, 1H), 5.22 (s, 2H), 4.20 (m, 1H), 4.11 (m, 1H), 4.04 (m, 1H), 3.72 (m, 2H), LCMS RT=3.32 min, [M+H]+=526.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07750017B2
Source datasetuspto-grants-2010_07
ORD IDord-ba90d51ac70b4fbb900818a20af79c50
Source noteuspto-grants-2010_07