HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437666Generated: October 30, 2026
Acetic Anhydride → HCID 21428838, compound
https://huagongshe.com/reaction/437666
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | HCID 21428956 | HCID 21428956 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21428838 | HCID 21428838 | — |
Reaction Steps
A mixture of 9 parts of 2-amino-4-fluoro-N-{2-[1-(4-fluorophenyl)-4-oxo-1,3,8-triazaspiro [4,5]dec-8-yl]ethyl}-benzamide, 8.5 parts of acetic acid anhydride and 85 parts of water is stirred for 30 minutes in a water-bath at about 80° C. The reaction mixture is cooled and alkalized with ammonium hydroxide. The product is extracted with trichloromethane. The aqueous phase is separated and extracted with trichloromethane. The combined organic phases are washed three times with water, dried, filtered and evaporated. The residue is crystallized from 2-propanol. The product is filtered off and dried, yielding 5.2 parts of 2-(acetylamino)-4-fluoro-N-{2-[1-(4-fluorophenyl)-4-oxo-1,3,8-triazaspiro-[4,5]dec-8-yl]ethyl}benzamide; mp. 195.1° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04031226 |
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| Source dataset | uspto-grants-1977_06 |
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| ORD ID | ord-9c012fbcba10462e81db522f563a513b |
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| Source note | uspto-grants-1977_06 |
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