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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1429509Generated: November 2, 2026

(2R)-1-amino-3-(1,2,3,4-tetrahydroisoquinolin-2-yl)propan-2-ol → (R)-N-(3-(3,4-dihydroisoquinolin-2(1H)-yl)-2-hydroxypropyl)-2-((2-methoxyquinolin-8-yl)oxy)acetamide

https://huagongshe.com/reaction/1429509

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2R)-1-amino-3-(1,2,3,4-tetrahydroisoquinolin-2-yl)propan-2-olHCID 25312351—
ReactantEthyl 2-((2-methoxyquinolin-8-yl)oxy)acetateHCID 90237870—
SolventEthanolHCID 702—
Product(R)-N-(3-(3,4-dihydroisoquinolin-2(1H)-yl)-2-hydroxypropyl)-2-((2-methoxyquinolin-8-yl)oxy)acetamideHCID 9024190348%

Reaction Conditions

Temperature120 °C

Reaction Steps

Ethyl 2-((2-methoxyquinolin-8-yl)oxy)acetate (100 mg, 0.383 mmol), (R)-1-amino-3-(3,4-dihydroisoquinolin-2(1H)-yl)propan-2-ol (79.0 mg, 0.383 mmol) and EtOH (1 mL) were combined in a sealed tube. The mixture was stirred at 120° C. for 30 min in a microwave. The EtOH was evaporated and the residue was purified by pre-HPLC to give the desired product (77 mg, yield 48%). 1HNMR (MeOD-d4, 400 MHz) δ: 8.36 (br. s., 1H), 8.16 (d, J=8.8 Hz, 1H), 7.51 (d, J=7.5 Hz, 1H), 7.36 (t, J=7.9 Hz, 1H), 7.28-7.15 (m, 4H), 7.12 (d, J=6.8 Hz, 1H), 7.03 (d, J=8.8 Hz, 1H), 4.82 (s, 2H), 4.23-4.16 (m, 3H), 4.10 (s, 3H), 3.54-3.48 (m, 1H), 3.47-3.40 (m, 1H), 3.38-3.33 (m, 2H), 3.13-2.98 (m, 4H). LCMS (m/z): 422.2 [M+H]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940726B2
Source datasetuspto-grants-2015_01
ORD IDord-8a53cef65e1a49f0bde7778292e95e76
Source noteuspto-grants-2015_01