Réaction #632024

ord-18e4d16b5a1e403d87173367c2a8a774

Équation de réaction

CC1(C)COC2(CCCc3ncc([N+](=O)[O-])cc3CC2)OC1
5′,5′-dimethyl-3-nitro-6,8,9,10-tetrahydro-5H-spiro[cycloocta[b]pyridine-7,2′-[1,3]dioxane]
CC1(C)COC2(CCCc3ncc(N)cc3CC2)OC1
5′,5′-dimethyl-6,8,9,10-tetrahydro-5H-spiro[cycloocta[b]pyridine-7,2′-[1,3]dioxan]-3-amine

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Mode opératoire

The compound of formula (Cc), 5′,5′-dimethyl-3-nitro-6,8,9,10-tetrahydro-5H-spiro[cycloocta[b]pyridine-7,2′-[1,3]dioxane], was hydrogenated in ethanol/THF solution over 10% Pd/C for 1 hour at 40 psi to give the compound of formula (Cd), 5′,5′-dimethyl-6,8,9,10-tetrahydro-5H-spiro[cycloocta[b]pyridine-7,2′-[1,3]dioxan]-3-amine, in quantitative yield; MS (ES) 277.67 (M+2H).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07935693B2uspto-grants-2011_05