Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Triethyl 2-phosphonopropionate | HCID 107155 | — |
| Reactant | HCID 18796731 | HCID 18796731 | — |
| Reactant | Ethanol hydrochloride | HCID 21887872 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 70108448 | HCID 70108448 | 40.1% |
Reaction Steps
0.52 g (0.013 mol) of sodium hydride was added to a solution of 4.00 g (0.0117 mol) of 2-formyl-4-(3,4-methylene dioxybenzyl)amino-6-chloroquinazoline in 250 ml of tetrahydrofuran. 2.8 ml (0.013 mol) of triethyl 2-phosphonopropionate was dropped into the mixture prepared above under stirring and cooling with ice. The mixture thus prepared was stirred under cooling with ice for a while, heated to room temperature and stirred for additional one hour, followed by the addition of 1.5 ml of 8M hydrochloric acid/ethanol. The obtained mixture was passed through a small amount of silica gel and distilled under a reduced pressure to remove the solvent. The residue was purified by silica gel column chromatography (ethyl acetate/n-hexane) and recrystallized from chloroform/n-hexane to give 2.00 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06046206 |
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| Source dataset | uspto-grants-2000_04 |
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| ORD ID | ord-dbb71ba2f0b44d9a9469ceae07189745 |
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| Source note | uspto-grants-2000_04 |
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