HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591861Generated: November 1, 2026
HCID 136415077, compound → HCID 135939081, compound
https://huagongshe.com/reaction/591861
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 136415077 | HCID 136415077 | — |
| Reactant | HCID 178418634 | HCID 178418634 | — |
| Product | HCID 135939081 | HCID 135939081 | — |
Reaction Steps
2-[3-(2-Azido-ethoxy)-5-methoxy-phenyl]-5,7-dimethoxy-3H-quinazolin-4-one (90 mg, 0.22 mmol) was taken in thioacetic acid (2 mL) and the reaction mixture was stirred at room temperature for 2 hours. Thioacetic acid was removed under reduced pressure, and the residue was purified by column chromatography (silica gel 230-400 mesh; 3.5% methanol in dichloromethane as eluent) to give the title compound as a white solid. Yield: 45 mg (49%). MP 264-265° C. 1H NMR (400 MHz, DMSO-d6): δ 12.05 (s, 1H), 8.13 (t, J=5.86 Hz, 1H), 7.39 (d, J=1.56 Hz, 2H), 6.76 (d, J=2.34 Hz, 1H), 6.69 (t, J=2.15 Hz, 1H), 6.55 (d, J=2.34 Hz, 1H), 4.07 (t, J=5.67 Hz, 2H), 3.90 (s, 3H), 3.85 (s, 3H), 3.83 (s, 3H), 3.43 (q, J=5.47 Hz, 2H), 1.84 (s, 3H). MS (ES+) m/z: 414.11 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09238640B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-8209a409242b420a805eeda393b308e9 |
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| Source note | uspto-grants-2016_01 |
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