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HRID 12829Erstellt: 23. Oktober 2026

2-Aminoadamantane hydrochloride → 2'-methyl-2'H-[1,3']bipyrazolyl-4'-carboxylic acid adamantan-2-ylamide

https://huagongshe.com/de/reaction/12829

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Aminoadamantane hydrochlorideHCID 25331—
EduktDiisopropylethylamineHCID 81531—
Edukt2-(2,5-Dioxopyrrolidin-1-yl)-1,1,3,3-tetramethylisouronium tetrafluoroborateHCID 9857522—
Edukt2'-methyl-2'H-[1,3']bipyrazolyl-4'-carboxylic acidHCID 58972849—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
Produkt2'-methyl-2'H-[1,3']bipyrazolyl-4'-carboxylic acid adamantan-2-ylamideHCID 2501354177%

Reaktionsschritte

2′-Methyl-2′H-[1,3′]bipyrazolyl-4′-carboxylic acid (Intermediate 8, 50 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 phases were dried under vacuum and purified by C-18 reversed phase prep-HPLC with a gradient of 10-100% acetonitrile/water to give 2′-methyl-2′H-[1,3′]bipyrazolyl-4′-carboxylic acid adamantan-2-ylamide (65 mg, 77%). Mass spectrum: m/z: 362.2 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07728029B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-e39314f40e6043cb9d02def678859e3f
Quellennotizuspto-grants-2010_06