HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 631257Generated: October 26, 2026
Phosphorus oxychloride → 4-Chloro-7-(3-chloropropoxy)-6-methoxyquinazoline
https://huagongshe.com/reaction/631257
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 7-(3-chloropropoxy)-6-methoxy-1H-quinazolin-4-one | HCID 178486769 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-Chloro-7-(3-chloropropoxy)-6-methoxyquinazoline | HCID 57447227 | 78% |
Reaction Steps
To a solution of the intermediate from Step 4 (3.00 g, 11.16 mmol) in toluene (30 mL) in a pressure vessel was added phosphorous oxychloride (8 mL). The mixture was heated to 125° C. for 5 hours. Completion of the reaction was monitored by LCMS. The mixture was concentrated to dryness and excess ethyl acetate was added. The solution was washed with water and brine and was dried (Na2SO4) and concentrated to afford the pure compound 4-chloro-7-(3-chloro-propoxy)-6-methoxy-quinazoline (2.51 g, 78%) as a yellow solid. 1H NMR (300 MHz, DMSO-d6) δ 8.85 (s, 1H), 7.48 (s, 1H), 7.35 (s, 1H), 4.35 (t, 2H), 4.00 (s, 3H), 3.75 (t, 2H), 2.25 (q, 2H). LC-MS (ESI)m/z 287 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09320739B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-bd76335f28a84b6c96c4d33b08f4f83e |
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| Source note | uspto-grants-2016_04 |
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