Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | HCID 58824134 | HCID 58824134 | — |
| Solvent | Ethanol hydrochloride | HCID 21887872 | — |
| Product | HCID 11349226 | HCID 11349226 | — |
Reaction Steps
4-[1-(3-Fluoro-benzyl)-7-methoxy-2-oxo-1,2,3,4-tetrahydro-quinazolin-5-yl]-piperazine-1-carboxylic acid tert-butyl ester (43 mg) was dissolved in 4 mL 2N HCl/ethanol and heated to 80° C. for 20 minutes. The reaction mixture was cooled to room temperature, and ether was added, precipitating 18 mg of 1-(3-fluoro-benzyl)-7-methoxy-5-piperazin-1-yl-3,4-dihydro-1H-quinazolin-2-one. MS: 371 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07196087B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-5666f9905b34459eba89312cb4cc9b63 |
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| Source note | uspto-grants-2007_03 |
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