HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577366Generated: October 28, 2026
Formamidine acetate → 6-Methoxy-7-((1-methylpiperidin-4-yl)methoxy)quinazolin-4(3H)-one
https://huagongshe.com/reaction/577366
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formamidine acetate | HCID 160693 | — |
| Reactant | Ethyl 2-amino-5-methoxy-4-((1-methylpiperidin-4-yl)methoxy)benzoate | HCID 21874813 | — |
| Solvent | 2-Methoxyethanol | HCID 8019 | — |
| Product | 6-Methoxy-7-((1-methylpiperidin-4-yl)methoxy)quinazolin-4(3H)-one | HCID 135470375 | 83.7% |
Reaction Steps
A solution of ethyl 6-amino-3-methoxy-4-(1-methylpiperidin-4-ylmethoxy)benzoate (16.1 g, 50 mmol) in 2-methoxyethanol (160 ml) containing formamidine acetate (5.2 g, 50 mmol) was heated at 115° C. for 2 hours. Formamidine acetate (10.4 g, 100 mmol) was added in portions every 30 minutes over 4 hours. Heating was prolonged for 30 minutes after the last addition. After cooling, the volatiles were removed under vacuum. The solid was dissolved in ethanol (100 ml) and methylene chloride (50 ml). The precipitate was removed by filtration and the filtrate was concentrated to a final volume of 100 ml. The suspension was cooled to 5° C. and the solid was collected by filtration, washed with cold ethanol followed by ether and dried under vacuum overnight at 60° C. to give 6-methoxy-7-(1-methylpiperidin-4-ylmethoxy)-3,4-dihydroquinazolin-4-one (12.7 g, 70%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09040548B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-02f708c26ba446c18d4565c5b8a75eaf |
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| Source note | uspto-grants-2015_05 |
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