Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506561Generated: October 31, 2026

Ethanolamine → HCID 67172602, compound

https://huagongshe.com/reaction/1506561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolamineHCID 700—
Reactant4-MethylmorpholineHCID 7972—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
ReactantHCID 67171061HCID 67171061—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
ProductHCID 67172602HCID 6717260229.6%

Reaction Steps

To 2-hydroxy-2-(3-(5-phenyl-4-(trifluoromethyl)isoxazol-3-yl)-4,5-dihydronaphtho[1,2-c]isoxazol-7-yl)propanoic acid (Preparation 134D, isomer 1, 15 mg, 0.032 mmol) in DMF (1 mL) was added 2-aminoethanol (2.9 mg, 0.048 mmol), BOP (18.3 mg, 0.041 mmol) and 4-methylmorpholine (12.9 mg, 0.13 mmol). The reaction mixture was stirred for 1 h. Methanol was added and it was purified by prep HPLC (Phenomenex Luna 5 u 21.2×100 mm, Solvent A: 90% water with 10% acetonitrile and 0.1% TFA, Solvent B: 90% acetonitrile with 10% water and 0.1% TFA, Gradient: 0% B to 100% B over 10 min, 20 mL/min, 220 nM) to yield 2-hydroxy-N-(2-hydroxyethyl)-2-(3-(5-phenyl-4-(trifluoromethyl)isoxazol-3-yl)-4,5-dihydronaphtho[1,2-c]isoxazol-7-yl)propanamide (5 mg, 9.45 μmol, 29.6% yield): product HPLC ret. time=9.07 min (condition G); LC/MS M+1=514.16; 1H NMR (400 MHz, CD3OD) δ ppm 7.91 (1H, d, J=7.92 Hz), 7.77 (2H, d, J=7.26 Hz), 7.58-7.71 (5H, m), 3.60 (2H, td, J=5.72, 3.30 Hz), 3.33-3.41 (2H, m), 3.07 (4H, s), 1.78 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216972B2
Source datasetuspto-grants-2015_12
ORD IDord-4829d323b7774f5d9fbc49e56218fa63
Source noteuspto-grants-2015_12