HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1429458Generated: October 31, 2026
HCID 354312, compound → HCID 90241632, compound
https://huagongshe.com/reaction/1429458
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 354312 | HCID 354312 | — |
| Reactant | 1-amino-3-(3,4-dihydroisoquinolin-2(1H)-yl)propan-2-ol | HCID 16790720 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 90241632 | HCID 90241632 | 25% |
Reaction Steps
To a stirred mixture of ethyl 2-(3-carbamoylphenoxy)acetate (150 mg, 0.673 mmol) in EtOH (1 mL) was added 1-amino-3-(3,4-dihydroisoquinolin-2(1H)-yl)propan-2-ol (138.6 mg, 0.673 mmol). The mixture was stirred at 120° C. for 0.5 hour under mediated heating. After evaporation of the solvent, the residue was purified by prep-HPLC to afford the desired title product (64 mg, Yield 25%). 1H NMR (400 MHz, MeOD) δ 7.53 (d, J=8.0 Hz, 1H), 7.48 (s, 1H), 7.39 (dd, J1=J2=7.9 Hz, 1H), 7.12-7.00 (m, 5H), 4.60 (s, 2H), 4.04-4.01 (m, 1H), 3.74-3.65 (m, 2H), 3.47-3.39 (m, 2H), 2.95-2.87 (m, 2H), 2.85-2.77 (m, 2H), 2.58 (d, J=6.0 Hz, 2H). LCMS (m/z): 384.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08940726B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-ebd7e96c57aa4441b587cded92d90011 |
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| Source note | uspto-grants-2015_01 |
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