HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 428429Generated: October 29, 2026
HCID 18358856, compound → HCID 178520047, compound
https://huagongshe.com/reaction/428429
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 18358856 | HCID 18358856 | — |
| Reactant | HCID 18358913 | HCID 18358913 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178520047 | HCID 178520047 | 9% |
Reaction Steps
A solution of 1-(4-methoxyphenylmethyl)-7-chloro-3-formylpyrazolo[3,4-c][1]benzazepine-4,10(1H,9H)-dione or 2-(4-methoxyphenylmethyl)-7-chloro-3-formylpyrazolo[3,4-c][1]benzazepine-4,10(2H,9H)-dione from Example 20(b) above (400 mg, 1.01 mmol) and ceric ammonium nitrate (2.2 g, 4.03 mmol) in a mixture of acetonitrile (12 mL) and water (4 mL) was stirred for 17 hours at room temperature and filtered. The isolated solid was washed with a mixture of acetonitrile (12 ml,) and water (4 mL) followed by acetone (10 mL). The acetonitrile-water solutions were extracted with ethyl acetate. The solid material from above was combined with the ethyl acetate extract and solvent was removed by rotary evaporation. The residue was washed with hot methanol (1×20 mL then 1×10 mL) and dried to give the title Compound (25 mg, 9%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06313290B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-ddf1575bf10e455d916f70af90a25d86 |
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| Source note | uspto-grants-2001_11 |
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