HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538905Generated: November 1, 2026
Formamidine acetate → 7-Benzyloxy-6-methoxy-3H-quinazolin-4-one
https://huagongshe.com/reaction/538905
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formamidine acetate | HCID 160693 | — |
| Reactant | Benzyl 2-amino-4-(benzyloxy)-5-methoxybenzoate | HCID 11057568 | — |
| Solvent | Isobutanol | HCID 6560 | — |
| Product | 7-Benzyloxy-6-methoxy-3H-quinazolin-4-one | HCID 135404718 | — |
Reaction Steps
Benzyl 2-amino-4-(benzyloxy)-5-methoxybenzoate (80.0 g), formamidine acetate (32.0 g) and isobutanol (480 ml) were mixed. The reaction mixture was then heated to 97° C. and stirred at this temperature for 6 hours. The reaction mixture was then cooled to 25° C. over a period of at least an hour and then stirred at this temperature for 30 minutes. The product (7-benzyloxy-6-methoxy-3,4-dihydroquinazolin-4-one) was isolated by filtration, washed with isobutanol (64.2 g) and dried in the vacuum oven at a temperature of from 40 to 45° C. Yield: 60.8 g, 98%; NMR Spectrum (DMSOd6) 3.9 (s, 3H), 5.3 (s, 2H), 7.3 (s, 1H), 7.3-7.5 (m, 6H), 8.0 (s, 1H); Mass Spectrum (M+H)+=283.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08865899B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-85093ba7d799469db7885e04d5090313 |
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| Source note | uspto-grants-2014_10 |
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