Reacción #42201

ord-037b887922de407fbf568451c5ed7526

Ecuación de reacción

COS(=O)(=O)c1ccc(C)cc1
Intermediate 7
COS(=O)(=O)c1ccc(C)cc1
methyl 4-methylbenzenesulfonate
NCC1Cc2ccc3c(c2O1)CCCC3
(±)-1-(2,3,6,7,8,9-hexahydronaphtho[1,2-b]furan-2-yl)methanamine
CCN(C(C)C)C(C)C
diisopropylethylamine
O=C(Cl)OCc1ccccc1
benzyl chloroformate
O=C(NCC1Cc2ccc3c(c2O1)CCCC3)OCc1ccccc1
(±)-benzyl 2,3,6,7,8,9-hexahydronaphtho[1,2-b]furan-2-ylmethylcarbamate
Rendimiento 79.1%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Procedimiento

Treatment of (±)-1-(2,3,6,7,8,9-hexahydronaphtho[1,2-b]furan-2-yl)methanamine (0.846 g, 4.16 mmol) with diisopropylethylamine (0.592 g, 4.58 mmol) followed by benzyl chloroformate (0.745 g, 4.37 mmol) generally according to the procedure described for Intermediate 7 provided 1.11 g (79%) of (±)-benzyl 2,3,6,7,8,9-hexahydronaphtho[1,2-b]furan-2-ylmethylcarbamate as a white solid. Rf=0.39 (silica, ethyl acetate:hexanes 1:4); mp 88-90° C.; 1H NMR (DMSO-d6) δH 7.49 (t, 1H); 7.33 (m, 4H); 6.87 (d, 1H); 6.50 (d, 1H); 5.02 (s, 2H); 4.76 (m, 1H); 3.20 (m, 3H); 2.83 (dd, 1H); 2.62 (s, 2H); 2.49 (m, 2H); 1.67 (m, 4H). Chiral HPLC separation of (±)-benzyl 2,3,6,7,8,9-hexahydronaphtho[1,2-b]furan-2-ylmethylcarbamate (Chiralcel OJ, isopropanol:hexane 9:1) provided two fractions. Fraction 1 (Rt=11.576 min, Chiralcel OD, isopropanol:hexanes 1:9); Fraction 2 (Rt=14.729 min, Chiralcel OD, isopropanol:hexanes 1:9).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07728155B2uspto-grants-2010_06