HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437887Generated: November 3, 2026
Trifluoroacetic acid → (4r,7s)-2-(2,4-Difluoro-phenyl)-7,8,8-trimethyl-1,2,4,5,6,7-hexahydro-4,7-methano-indazol-3-one
https://huagongshe.com/reaction/1437887
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | n'-(2,4-Difluoro-phenyl)-n'-((1s,4s)-4,7,7-trimethyl-3-oxo-bicyclo[2.2.1]heptane-2-carbonyl)-hydrazinecarboxylic acid tert-butyl ester | HCID 57941383 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (4r,7s)-2-(2,4-Difluoro-phenyl)-7,8,8-trimethyl-1,2,4,5,6,7-hexahydro-4,7-methano-indazol-3-one | HCID 57941350 | 84.5% |
Reaction Steps
Trifluoroacetic acid (80 mL) was added to a solution of crude N′-(2,4-difluoro-phenyl)-N′-((1S,4S)-4,7,7-trimethyl-3-oxo-bicyclo[2.2.1]heptane-2-carbonyl)-hydrazinecarboxylic acid tert-butyl ester (˜100 mmol) in dichloromethane (80 mL) at 0° C. The reaction mixture was stirred at 0° C. for 15 min, and then at room temperature for 4 h. The solvent was evaporated. The residue was taken up in dichloromethane (500 mL) and washed with water (4×600 mL) adding brine to help separate the layers when necessary. The solution was further washed with brine (250 mL), dried (magnesium sulfate), filtered, and evaporated. The solids were triturated with 10% dichlormethane/hexanes, filtered, washed with 5% dichloromethane/hexanes and then hexanes, stored over a weekend in the freezer, and then dried under high vacuum to give (4R,7S)-2-(2,4-difluoro-phenyl)-7,8,8-trimethyl-1,2,4,5,6,7-hexahydro-4,7-methano-indazol-3-one (25.71 g, 84%) as a light brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07622492B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-cafffd75f1434087b96886418701689f |
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| Source note | uspto-grants-2009_11 |
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