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HRID 12830Erstellt: 23. Oktober 2026

2-Aminoadamantane hydrochloride → 1-methyl-5-trifluoromethyl-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide

https://huagongshe.com/de/reaction/12830

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Aminoadamantane hydrochlorideHCID 25331—
EduktDiisopropylethylamineHCID 81531—
Edukt1-Methyl-5-(trifluoromethyl)pyrazole-4-carboxylic AcidHCID 2807771—
Edukt2-(2,5-Dioxopyrrolidin-1-yl)-1,1,3,3-tetramethylisouronium tetrafluoroborateHCID 9857522—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
Produkt1-methyl-5-trifluoromethyl-1H-pyrazole-4-carboxylic acid adamantan-2-ylamideHCID 2501354265%

Reaktionsschritte

Methyl-5-trifluoromethyl-1H-pyrazole-4-carboxylic acid (77 mg, 0.4 mmol, CAS#: 119083-00-0, purchased from Bionet) was dissolved in a mixture of dry dichloromethane (3.2 mL) and dry DMF (0.8 mL). DIPEA (0.28 mL, 1.6 mmol) and TSTU (145 mg, 0.44 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 (75 mg, 0.4 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 phases were dried under vacuum and purified by C-18 reversed phase HPLC with a gradient of 10-100% acetonitrile/water to give 1-methyl-5-trifluoromethyl-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide (85 mg, 65%). Mass spectrum: m/z: 328.2 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07728029B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-b7c63b53a9564e1ea614af812d6e8e45
Quellennotizuspto-grants-2010_06