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HRID 75157Erstellt: 23. Oktober 2026

Tricyclo(3.3.1.13,7)dec-1-ylmethylamine → HCID 59437175, Verbindung

https://huagongshe.com/de/reaction/75157

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTricyclo(3.3.1.13,7)dec-1-ylmethylamineHCID 86625—
Edukt(S)-tert-butyl 2-(t-butyldimethylsilyloxymethyl)aziridine-1-carboxylateHCID 72525716—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 59437175HCID 5943717542,5%

Reaktionsschritte

To a solution of (1-adamantylmethyl)amine (15 g, 52 mmol) in anhydrous CH2Cl2 (50 mL) was added tert-butyl 2-((tert-butyldimethylsilyloxy)methyl)aziridine-1-carboxylate (13 g, 78.3 mmol). The mixture was stirred for 10 min, the solvent was removed in vacuo and the residue was stirred at 40° C. for 5 h. The mixture was diluted with EtOAc (500 mL) and washed with water (100 mL),1N aq HCl (50 mL), satd aq NaHCO3 (50 ml) and brine (50 mL), and dried over MgSO4. The solution was concentrated to give a residue, which was purified by chromatography on silica gel to give (S)-tert-butyl 1-(tert-butyldimethylsilyloxy)-3-((1-adamantylmethyl)amino)propan-2-ylcarbamate (10 g, 24%). 1H NMR: (CDCl3, 400 MHz): δ=0.041 (s, 6H), 0.882 (s, 9H), 1.44 (s, 9H), 1.49 (s, 6H), 1.65 (m, 6H), 1.94 (s, 3H), 2.23 (s, 2H), 2.62-2.81 (m, 2H), 3.67 (m, 3H), 5.30 (s, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08835426B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-b12f6b0d30474bdbb69a09795a73ce18
Quellennotizuspto-grants-2014_09