HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 386598Generated: October 26, 2026
Water → 3-benzyl-6-(1,4-dioxa-spiro[4.5]dec-8-yloxy)-7-methoxy-3H-quinazolin-4-one
https://huagongshe.com/reaction/386598
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,4-Dioxaspiro(4.5)decan-8-yl methanesulfonate | HCID 14966741 | — |
| Reactant | 3-Benzyl-6-hydroxy-7-methoxyquinazolin-4-one | HCID 16734939 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-benzyl-6-(1,4-dioxa-spiro[4.5]dec-8-yloxy)-7-methoxy-3H-quinazolin-4-one | HCID 58157254 | — |
Reaction Steps
16.0 g potassium carbonate and 20.0 g 8-methanesulphonyloxy-1,4-dioxa-spiro[4.5]decan are added at 50° C. to 20.0 g 3-benzyl-3,4-dihydro-4-oxo-6-hydroxy-7-methoxy-quinazoline in 150 ml N,N-dimethylformamide and the mixture is vigorously stirred for 18 hours at 80° C. To complete the reaction potassium carbonate and 8-methanesulphonyloxy-1,4-dioxa-spiro[4.5]decan are each added three times and in each case the mixture is stirred for several hours at 80° C. The reaction mixture is cooled and slowly combined with a total of 500 ml of water. The precipitate is suction filtered, washed with water and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08372855B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-f661c0a74a9c41aea1d7d3d666c0fe8f |
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| Source note | uspto-grants-2013_02 |
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