HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2106102Generated: October 30, 2026
Phenylacetyl isothiocyanate → 1-[6-(6,7-Dimethoxy-quinolin-4-yloxy)-pyridin-3-yl]-3-phenylacetyl-thiourea
https://huagongshe.com/reaction/2106102
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phenylacetyl isothiocyanate | HCID 12454157 | — |
| Reactant | 6-(6,7-Dimethoxyquinolin-4-yloxy)pyridin-3-amine | HCID 22936597 | — |
| Solvent | Ethylacetate methanol | HCID 21584119 | — |
| Product | 1-[6-(6,7-Dimethoxy-quinolin-4-yloxy)-pyridin-3-yl]-3-phenylacetyl-thiourea | HCID 11340470 | 298.7% |
Reaction Steps
To a round bottom flask equipped with a magnetic stir bar was added 6-(6,7-dimethoxy-quinolin-4-yloxy)-pyridin-3-ylamine (85 mg, 0.0285 mmol, 1.0 eq.), and Phenyl-acetyl isothiocyanate (256 mg, 1.44 mmol, 5.0 eq.) dissolved in EtOAc/MeOH 50:50 (2 mL). The reaction mixture was stirred at room temperature for 12 hours, and the solvent was evaporated via rotary evaporation. Purification was done on Biotage with solvent system 95% EtOAc, 4% TEA and 1% MeOH. The combined pure fractions were concentrated and dried under vacuum overnight to yield 1-[6-(6,7-dimethoxy-quinolin-4-yloxy)-pyridin-3-yl]-3-phenylacetyl-thiourea as a light yellow solid (40.4 mg, 29.7%). 1H NMR (400 MHz, CDCl3): 8.65 (d, 1H), 8.33 (d, 1H), 8.27 (dd, 1H), 7.35 (m, 7H), 7.15 (d, 1H), 6.92 (d, 1H), 4.05 (s, 3H), 3.99 (s, 3H), 3.76 (s, 2H); MS (EI) for C25H22N4O4S: 475 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07579473B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-227fbc0bcf194ca6adf926b8898ec481 |
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| Source note | uspto-grants-2009_08 |
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