HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 890969Generated: October 29, 2026
Trifluoroacetic acid → HCID 178486737, compound
https://huagongshe.com/reaction/890969
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 178486734 | HCID 178486734 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178486737 | HCID 178486737 | 67% |
Reaction Steps
A mixture of N-(tert-butoxycarbonylmethyl)-N′-(2,6-dimethylphenyl)-N″-[6-methoxy-7-(N-methylpiperidin-4-ylmethoxy)quinazolin-4-yl]guanidine (0.09 g), trifluoroacetic acid (1 ml) and methylene chloride (1 ml) was stirred at ambient temperature for 3 hours. The reaction mixture was evaporated and the residue was purified by column chromatography on silica using increasingly polar mixture of methylene chloride and a 2M solution of ammonia gas in methanol as eluent. There was thus obtained the title compound in 67% yield: NMR Spectrum: (DMSOd6, 100° C.) 1.2–1.5 (m, 3H), 1.7–1.9 (m, 2H), 2.0–2.1 (m, 2H), 2.14 (s, 3H), 2.19 (s, 6H), 2.84 (d, 2H), 3.82 (s, 3H), 3.95–4.05 (m, 4H), 7.08 (s, 1H), 7.17 (s, 3H), 7.71 (s, 1H), 8.43 (s, 1H); Mass Spectrum: M+H+ 507.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07001904B1 |
|---|
| Source dataset | uspto-grants-2006_02 |
|---|
| ORD ID | ord-6f845cde990742d2bbba03c08f4b124b |
|---|
| Source note | uspto-grants-2006_02 |
|---|