Reacción #2267085

Ecuación de reacción

sodium cyanoborohydride

2-(2,3-dihydro[1,4]oxazino[2,3,4-hi]indol-6-ylmethyl)-1H-isoindole-1,3(2H)-dione

NaOH

→

title compound

(rac)-2-(2,3,5,6-tetrahydro[1,4]oxazino[2,3,4-hi]indol-6-ylmethyl)-1H-isoindole-1,3(2H)-dione

Disolventes

H2O

CH3OH

TFA

Condiciones de reacción

Tratamiento posterior

1. 1
   ExtracciónThe mixture was then extracted with EtOAc (3×)
2. 2
   SecadoThe combined EtOAc solution was dried over MgSO4
3. 3
   Concentraciónconcentrated in vacuo to dryness
4. 4
   workup.DISSOLUTIONThe residue was redissolved in CH2Cl2
5. 5
   Filtraciónfiltered
6. 6
   ConcentraciónThe filtrate was concentrated in vacuo to dryness

Procedimiento

A freshly prepared solution of sodium cyanoborohydride (0.093 g, 1.48 mmol) in CH3OH (0.3 mL) was added dropwise to a 0° C. solution of 2-(2,3-dihydro[1,4]oxazino[2,3,4-hi]indol-6-ylmethyl)-1H-isoindole-1,3(2H)-dione (0.094 g, 0.29 mmol) in TFA (3.0 mL). The mixture was stirred at rt for 1 hour and diluted with H2O (10.0 mL) and made basic by the addition of 15% NaOH. The mixture was then extracted with EtOAc (3×). The combined EtOAc solution was dried over MgSO4 and concentrated in vacuo to dryness. The residue was redissolved in CH2Cl2 and filtered. The filtrate was concentrated in vacuo to dryness and the residue was subjected to preparative TLC (EtOAc/Hex., ½) to give 0.031 g (33%) of light yellow oil as the title compound: 1H NMR (400 MHz, CDCl3) δ 7.93-7.88 (m, 2 H), 7.80-7.75 (m, 2 H), 6.79-6.77 (m, 1 H), 6.75-6.65 (m, 2 H), 4.46-4.43 (m, 2 H), 4.10-4.05 (m, 1 H), 4.00-3.94 (m, 1 H), 3.77-3.73 (m, 1 H), 3.34-3.33 (m, 1 H), 3.30-3.26 (m, 1 H), 3.17-3.15 (m, 1 H), 3.10-3.08 (m, 1 H); MS (EI) m/z 321 (M++H).

Fuente