HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597252Generated: November 3, 2026
Triphenylphosphine → 7-(3-(1,1-Dioxothiomorpholino)propoxy)4-(2-methoxyethylsulphanyl)quinazoline
https://huagongshe.com/reaction/1597252
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | 4-(3-Hydroxypropyl)thiomorpholine 1,1-Dioxide | HCID 11435473 | — |
| Reactant | 7-Hydroxy-4-(2-methoxyethylsulphanyl)quinazoline | HCID 135798751 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 7-(3-(1,1-Dioxothiomorpholino)propoxy)4-(2-methoxyethylsulphanyl)quinazoline | HCID 69462762 | 41.7% |
Reaction Steps
Diethyl azodicarboxylate (100 μl; 0.63 mmol) was added dropwise to a solution of 7-hydroxy-4-(2-methoxyethylsulphanyl)quinazoline (100 mg, 0.42 mmol), (prepared as described for the starting material in Example 11), 3-(1,1-dioxothiomorpholino)-1-propanol (99 mg, 0.51 mmol) and triphenylphosphine (167 mg, 0.63 mmol) in methylene chloride (6 ml). After stiring for 4 hours, triphenylphosphine (167 mg, 0.63 mmol) and diethyl azodicarboxylate (100 μl, 0.63 mmol) were added and stirring was continued for 1 hour. The volatiles were removed by evaporation and the residue was purified by column chromatography eluting with ethyl acetate/methanol (100/0 followed by 92/8). After removal of the solvent by evaporation, the residue was triturated with ether and the solid was collected by filtration and dried under vacuum to give 7-(3-(1,1-dioxothiomorpholino)propoxy)4-(2-methoxyethylsulphanyl)quinazoline (72 mg, 41%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06294532B1 |
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| Source dataset | uspto-grants-2001_09 |
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| ORD ID | ord-5b08e7463a6d48068e245111785944e6 |
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| Source note | uspto-grants-2001_09 |
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