HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 641726Generated: October 31, 2026
Trifluoroacetic acid → HCID 22140839, compound
https://huagongshe.com/reaction/641726
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 22140775 | HCID 22140775 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22140839 | HCID 22140839 | 93.1% |
Reaction Steps
A mixture of 4-(2-bromo-5-methoxyanilino)-5-[N-(tert-butoxycarbonyl)piperidin-4-ylmethoxy]quinazoline (0.108 g), trifluoroacetic acid (1 ml) and methylene chloride (1 ml) was stirred at ambient temperature for 1.5 hours. The mixture was evaporated and the residue was triturated under diethyl ether. The resultant solid was isolated and dried under vacuum. The solid was dissolved in methylene chloride and few drops of a saturated methanolic ammonia solution was added. The solution was poured onto a chromatography column filled with silica and eluted with a 97:3 mixture of methylene chloride and a saturated methanolic ammonia solution. There was thus obtained the title compound (0.082 g); NMR Spectrum: (CDCl3) 1.2-1.4 (m, 2H), 1.9 (d, 2H), 2.3 (m, 1H), 2.65 (t, 2H), 3.12 (d, 2H), 3.84 (s, 3H), 4.2 (d, 2H), 6.61 (m, 1H), 6.93 (d, 1H), 7.5 (d, 2H), 7.68 (m, 1H), 8.22 (d, 1H), 8.68 (s, 1H); Mass Spectrum: M+H+ 443 and 445.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07696214B2 |
|---|
| Source dataset | uspto-grants-2010_04 |
|---|
| ORD ID | ord-ba366ef3d6024d83a028f55a41b6c0ea |
|---|
| Source note | uspto-grants-2010_04 |
|---|