HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1683705Generated: October 25, 2026
Formic Acid → 1-(4-Formylaminopheny1)-3-formyl-4-methyl-7,8-methylenedioxy-3,4-dihydro-5H-2,3-benzodiazepine
https://huagongshe.com/reaction/1683705
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Gyki 52895 | HCID 3539 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Product | 1-(4-Formylaminopheny1)-3-formyl-4-methyl-7,8-methylenedioxy-3,4-dihydro-5H-2,3-benzodiazepine | HCID 19040707 | — |
Reaction Steps
To 6.0 ml (0.104 mol) of acetic anhydride 3.0 ml (0.08 mol) of 100% formic acid were added dropwise at 0° C. during 5 minutes while constant stirring. The stirring was continued at 50° C. for 15 minutes. Thereafter 1 g (3.3 mmol) of 1-(4-aminophenyl)-4-methyl-7,8-methylenedioxy-3,4-dihydro-5H-2,3-benzodiazepine was added to the thus-prepared mixed anhydride. The reaction mixture was stirred at 25° C. for 1.5 hours, then poured into ice-water, the precipitate formed was filtered, washed with 4×5 ml of distilled water and dried at 80° C. to give 0.80 g of raw product. After crystallization from 3 ml of ethyl acetate 0.65 g (56.2%) of the aimed product was obtained, m.p.: 193°-195° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05639751 |
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| Source dataset | uspto-grants-1997_06 |
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| ORD ID | ord-a8e6e1550e614f54a803090487433043 |
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| Source note | uspto-grants-1997_06 |
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