HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536487Generated: October 30, 2026
Acetic Acid → 1-(2-Fluorobenzyl)-1,4,5,6-tetrahydrocyclopenta[c]pyrazole-3-carboximidamide
https://huagongshe.com/reaction/536487
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 1-(2-Fluorobenzyl)-1,4,5,6-tetrahydrocyclopenta[c]pyrazole-3-carbonitrile | HCID 71285377 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-(2-Fluorobenzyl)-1,4,5,6-tetrahydrocyclopenta[c]pyrazole-3-carboximidamide | HCID 86692092 | — |
Reaction Steps
Under nitrogen atmosphere, 3.600 g (14.92 mmol) of 1-(2-fluorobenzyl)-1,4,5,6-tetrahydrocyclopenta[c]pyrazole-3-carbonitrile was dissolved in 37 ml of absolute methanol. 1.306 g (24.17 mmol) of sodium methylate was added and it was stirred for 4 h at RT. 1.452 g (24.17 mmol) of acetic acid and 1.197 g (22.38 mmol) of ammonium chloride were added and the suspension was stirred overnight at 50° C. The reaction mixture was concentrated by evaporation and the residue was suspended in 100 ml water and 25 ml 1N hydrochloric acid. The mixture was extracted with dichloromethane. The aqueous phase was made basic (pH=12) with 2N sodium hydroxide solution and extracted three times with a mixture of dichloromethane/methanol (v/v=8:2). The combined organic phases were dried over sodium sulphate, concentrated by evaporation, toluene was added and again evaporated to dryness. 1.94 g (50% of theor.) of the target compound was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08859569B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-f283436204bf48b48dc611b8cc215d91 |
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| Source note | uspto-grants-2014_10 |
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