HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22781Generated: October 30, 2026
Trifluoroacetic acid → HCID 22591472, compound
https://huagongshe.com/reaction/22781
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 22591455 | HCID 22591455 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22591472 | HCID 22591472 | 59.9% |
Reaction Steps
A mixture of 7-(N-tert-butoxycarbonylpiperidin-4-ylmethoxy)-4-(6-chlorobenzofuran-7-ylamino)-6-methoxyquinazoline (0.4 g), trifluoroacetic acid (3 ml) and methylene chloride (12 ml) was stirred at ambient temperature for 3 hours. The mixture was evaporated and the residue was diluted with water. The mixture was basified to pH11 by the addition of 1 N aqueous sodium hydroxide solution and methylene chloride was added. The precipitate which was formed was collected by filtration, washed with water and dried under vacuum to give the title compound (0.195 g); NMR Spectrum: (DMSOd6 and CF3CO2D) 1.55 (m, 2H), 2.0 (m, 2H), 2.25 (m, 1H), 2.95 (m, 2H), 3.4 (m, 2H), 4.05 (s, 3H), 4.2 (d, 2H), 7.1 (d, 1H), 7.4 (s, 1H), 7.55 (d, 1H), 7.8 (d, 1H), 8.05 (d, 1H), 8.2 (s, 1H), 8.85 (s, 1H), Mass Spectrum: M−H− 437.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06849625B2 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-4ba40502caba4ec296e1b49588043d09 |
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| Source note | uspto-grants-2005_02 |
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