HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386281Generated: October 30, 2026
Dimethylformamide → 4-(7-Benzyloxyoxindol-3-yl)-6-methoxy-7-(3-morpholinopropoxy)quinazoline
https://huagongshe.com/reaction/1386281
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Chloro-6-methoxy-7-(3-morpholin-4-ylpropoxy)quinazoline | HCID 11823941 | — |
| Reactant | 7-Benzyloxyoxindole | HCID 21717230 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(7-Benzyloxyoxindol-3-yl)-6-methoxy-7-(3-morpholinopropoxy)quinazoline | HCID 21717199 | 58.6% |
Reaction Steps
Sodium hydride (36 mg, 1.5 mmol) was added in portions to a solution of 7-benzyloxyoxindole (360 mg, 1.5 mmol) in THF (8 ml), the mixture was stirred for 30 minutes at ambient temperature and a solution of 4-chloro-6-methoxy-7-(3-morpholinopropoxy)quinazoline (204 mg, 0.6 mmol), (prepared as described for the starting material in Example 5), in THF (4 ml) and DMF (1.5 ml) was added. The mixture was stirred for 30 minutes at ambient temperature followed by 1.5 hours at 65° C. The THF was removed by evaporation, the mixture was partitioned between ethyl acetate and water and the aqueous layer was adjusted to pH8 with 2M hydrochloric acid. The precipitated product was collected by filtration, washed with water, ethyl acetate, and ether, and dried under vacuum to give 4-(7-benzyloxyoxindol-3-yl)-6-methoxy-7-(3-morpholinopropoxy)quinazoline (190 mg, 58%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06265411B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-bf614ded2efb4a0f9632bbb96a78f103 |
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| Source note | uspto-grants-2001_07 |
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