HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 990992Generated: October 29, 2026
Aniline → 4-(1,4-Dihydroindeno[1,2-c]pyrazol-3-yl)benzanilide
https://huagongshe.com/reaction/990992
Participants
| Role | Name | HCID | Charge |
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| Reactant | Aniline | HCID 6115 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 4-(1,4-Dihydroindeno[1,2-c]pyrazol-3-yl)benzoic acid | HCID 18415847 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(1,4-Dihydroindeno[1,2-c]pyrazol-3-yl)benzanilide | HCID 18416000 | — |
Reaction Steps
A mixture of 4-(1,4-dihydroindeno[1,2-c]pyrazol-3-yl)benzoic acid (0.37 g), dichloromethane (20 ml) and oxalyl chloride (0.26 ml) was stirred at 15-20° C. and then dimethylformamide (3 drops) was added. The mixture was stirred at 15-20° C. for 30 minutes and then warmed at 40° C. for 1 hour. The solvent was removed under reduced pressure to give a solid which was dissolved in dichloromethane (20 ml) and then aniline (0.13 ml) and triethylamine (0.38 ml) were added. The mixture was stirred at ambient temperature under nitrogen for 2 hours and then washed with water, dried, filtered and evaporated to give a solid which was purified by flash column chromatography on silica to give 4-(1,4-dihydroindeno[1,2-c]pyrazol-3-yl)benzanilide, m.p. 186-190° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06462036B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-439c3b0e848345629d60be221d2b2ffc |
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| Source note | uspto-grants-2002_10 |
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