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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1777149Generated: October 31, 2026

1-amino-3-(3,4-dihydroisoquinolin-2(1H)-yl)propan-2-ol → HCID 178521389, compound

https://huagongshe.com/reaction/1777149

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-amino-3-(3,4-dihydroisoquinolin-2(1H)-yl)propan-2-olHCID 16790720—
ReactantHCID 178472961HCID 178472961—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductHCID 178521389HCID 17852138951%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of ethyl 2-(2-(1H-pyrazol-3-yl)phenoxy)acetate (100 mg, 0.41 mmol) in EtOH (10 mL) was added 1-amino-3-(3,4-dihydroisoquinolin-2(1H)-yl)propan-2-ol (84 mg, 0.41 mmol). The mixture was stirred at 120° C. under microwave heating for 2 h. The reaction mixture was diluted with ethyl acetate (30 mL) and washed with water (10 mL), dried over Na2SO4 and concentrated to give the crude product. The residue was purified by prep-HPLC to afford the desired title compound (85 mg, 44%). 1H NMR (400 MHz, MeOD): δ 7.71-7.69 (m, 2H), 7.34-7.33 (m, 1H), 7.10-7.01 (m, 6H), 6.74 (d, J=2 Hz, 1H), 4.67 (s, 1H), 4.04-4.02 (m, 1H), 3.67 (s, 2H), 3.50-3.49 (m, 1H), 3.37-3.33 (m, 1H), 2.89-2.87 (m, 2H), 2.81-2.78 (m, 2H), 2.58-2.57 (m, 2H) ppm; ESI-MS (m/z): 469.3 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266836B2
Source datasetuspto-grants-2016_02
ORD IDord-3dfd0df33ca142b09d703ce802309fca
Source noteuspto-grants-2016_02