Reacción #42233

ord-d9201732c96f4cf8a21d0dfa1a4626d8

Ecuación de reacción

COS(=O)(=O)c1ccc(C)cc1
Intermediate 7
COS(=O)(=O)c1ccc(C)cc1
methyl 4-methylbenzenesulfonate
NCC1Cc2cc(Cl)c3c(c2O1)CCC3
(±)-1-(5-chloro-3,6,7,8-tetrahydro-2H-indeno[4,5-b]furan-2-yl)methanamine
CCN(C(C)C)C(C)C
diisopropylethylamine
O=C(Cl)OCc1ccccc1
benzyl chloroformate
O=C(NCC1Cc2cc(Cl)c3c(c2O1)CCC3)OCc1ccccc1
(±)-benzyl (5-chloro-3,6,7,8-tetrahydro-2H-indeno[4,5-b]furan-2-yl)methylcarbamate
Rendimiento 84.0%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Procedimiento

Treatment of (±)-1-(5-chloro-3,6,7,8-tetrahydro-2H-indeno[4,5-b]furan-2-yl)methanamine (0.51 g, 1.96 mmol) with diisopropylethylamine (0.76 g, 5.88 mmol) followed by benzyl chloroformate (0.50 g, 2.94 mmol) generally according to the procedure described for Intermediate 7 provided 0.58 g (84%) of (±)-benzyl (5-chloro-3,6,7,8-tetrahydro-2H-indeno[4,5-b]furan-2-yl)methylcarbamate as a white solid. mp 118-121° C.; Anal. calcd. for C20H20ClNO3: C, 67.13; H, 5.63; N, 3.91. Found: C, 66.95; H, 5.93; N, 3.82. Chiral HPLC separation of (±)-benzyl (5-chloro-3,6,7,8-tetrahydro-2H-indeno[4,5-b]furan-2-yl)methylcarbamate (Chiralpak AD, hexane:isopropanol 9:1) provided two fractions. Fraction 1 (Rt=11.191 min, Chiralpak AD, hexane:isopropanol 9:1); Fraction 2 (Rt=12.735 min, Chiralpak AD, hexane:isopropanol 9:1).

Fuente

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