HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2084032Generated: October 31, 2026
HCID 22732266, compound → HCID 136116301, compound
https://huagongshe.com/reaction/2084032
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 22732266 | HCID 22732266 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 136116301 | HCID 136116301 | — |
Reaction Steps
A mixture of 7-benzyloxy-6-methoxy-4-[2-methyl-5-(2-morpholinopyridine-4-carboxamido)anilino]quinazoline dihydrochloride (4.45 g) and trifluoroacetic acid (20 ml) was stirred and heated to reflux for 90 minutes. The mixture was cooled to ambient temperature and evaporated. A mixture of a dilute aqueous sodium bicarbonate solution and methylene chloride was added to the residue and the resultant mixture was stirred for 30 minutes at ambient temperature. The precipitated solid was collected, washed with water and, dried under vacuum at 60° C. to give 7-hydroxy-6-methoxy-4-[2-methyl-5-(2-morpholinopyridine-4-carboxamido)anilino]quinazoline (3.67 g; NMR: 2.17 (s, 3H), 3.52 (t, 4H), 3.71 (t, 4H), 3.98 (s, 3H), 7.09 (d, 1H), 7.19 (s, 1H), 7.23 (s, 1H), 7.37 (d, 1H), 7.6 (d, 1H), 7.84 (s, 1H), 8.05 (s, 1H), 8.25 (d, 1H), 8.66 (s, 1H), 10.42 (s, 1H), 11.06 (s, 1H); m/s: M+H+ 487.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06716847B2 |
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| Source dataset | uspto-grants-2004_04 |
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| ORD ID | ord-53b73dae38c840189519b39108e89ae2 |
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| Source note | uspto-grants-2004_04 |
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