HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12832Generated: October 26, 2026
2-Aminoadamantane hydrochloride → 1-tert-butyl-5-trifluoromethyl-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide
https://huagongshe.com/reaction/12832
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Aminoadamantane hydrochloride | HCID 25331 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-tert-Butyl-5-(trifluoromethyl)-1H-pyrazole-4-carboxylic acid | HCID 1482039 | — |
| Reactant | 2-(2,5-Dioxopyrrolidin-1-yl)-1,1,3,3-tetramethylisouronium tetrafluoroborate | HCID 9857522 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-tert-butyl-5-trifluoromethyl-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide | HCID 25013544 | 65% |
Reaction Steps
tert-Butyl-5-trifluoromethyl-1H-pyrazole-4-carboxylic acid (Intermediate 7, 61 mg, 0.26 mmol) was dissolved in a mixture of dry dichloromethane (3.2 mL) and dry DMF (0.8 mL). DIPEA (0.23 mL, 1.3 mmol) and TSTU (93 mg, 0.28 mmol) were added to the above mixture. After the mixture was stirred for 1 h, the appearance of active ester was detected by LC-MS. Then 2-aminoadamantane hydrochloride (58 mg, 0.31 mmol) was added. After another 2 hours water was added and the organic layer was separated. The aqueous layer was extracted twice with dichloromethane. The combined organic layers were dried under vacuum and purified by C-18 reversed phase HPLC with a gradient of 10-100% acetonitrile/water to give 1-tert-butyl-5-trifluoromethyl-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide (62 mg, 65%). Mass spectrum: m/z: 370.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07728029B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-d53e24288b474cab86af0923b73f4cca |
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| Source note | uspto-grants-2010_06 |
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