HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 658117Generated: October 30, 2026
Acetic Anhydride → HCID 178474883, compound
https://huagongshe.com/reaction/658117
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 178511391 | HCID 178511391 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 178474883 | HCID 178474883 | 80% |
Reaction Steps
A 137 mg portion of 1-[3-(2-amino-1-hydroxyethyl)phenyl]-3-(3,5-difluorophenyl)-2-(1,3-dihydro-2H-benzimidazol-2-ylidene)propane-1,3-dione was dissolved in 10 ml of pyridine, and 35 mg of acetic anhydride was added thereto under ice-cooling. After 2.5 hours of stirring at room temperature, the reaction liquid was mixed with an appropriate amount of sodium bicarbonate aqueous solution, extracted with ethyl acetate, dried with anhydrous sodium sulfate and concentrated, and then the thus formed residue was purified by a silica gel column chromatography to obtain 120 mg (80%) of N-(2-{3-[3-(3,5-difluorophenyl)-2-(1,3-dihydro-2H-benzimidazol-2-ylidene)-3-oxopropanoyl]phenyl}-2-hydroxyethyl)acetamide (Example 15-1) as a yellow foam from a chloroform-methanol (30:1) eluate. FA: 478
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08076367B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-06a93773cd554bbdbf3245bc595203e5 |
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| Source note | uspto-grants-2011_12 |
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