HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247918Generated: November 2, 2026
Trimethyl orthoformate → 7-[(1H-imidazol-1-yl)phenylmethyl]-4(3H)-quinazolinone
https://huagongshe.com/reaction/2247918
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trimethyl orthoformate | HCID 9005 | — |
| Reactant | 2-amino-4-[(1H-imidazol-1-yl)phenylmethyl]benzamide | HCID 53875358 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | 7-[(1H-imidazol-1-yl)phenylmethyl]-4(3H)-quinazolinone | HCID 135981652 | 23.6% |
Reaction Steps
A mixture of 4.2 parts of 2-amino-4-[(1H-imidazol-1-yl)phenylmethyl]benzamide, 97 parts of trimethoxymethane and 1.3 parts of formic acid was stirred for 5 hours at reflux temperature and overnight at room temperature. The solvent was evaporated and the residue was dissolved in methanol. The solution was basified with ammonious methanol and then evaporated. The residue was purified twice by column chromatography (silica gel; CHCl3 /CH3OH 95:5; CHCl3 /CH3OH 90:10). The eluent of the desired fraction was evaporated and the residue was crystallized from acetonitrile. The product was filtered off, washed with 2,2'-oxybispropane and dried, yielding 1 part (23.6%) of 7-[(1H-imidazol-1-yl)phenylmethyl]-4(3H)-quinazolinone; mp. 205.0° C. (comp. 47).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05037829 |
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| Source dataset | uspto-grants-1991_08 |
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| ORD ID | ord-c45ecfedfefa4869809a3651c02319cc |
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| Source note | uspto-grants-1991_08 |
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