Water → HCID 59263478, compound

HRID 645275Notes

Reaction equation

HRID 645275 reaction equation
[CH2:1]([N:6]1[C:27]2[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=2)[C:8]2([CH2:20]C[C:18](=[O:21])[C:17]3[C:9]2=[CH:10][C:11]2[O:15][CH2:14][O:13][C:12]=2[CH:16]=3)[C:7]1=[O:28])[CH2:2][CH2:3][CH2:4][CH3:5].[BH4-].[Na+].O>CO>[OH:21][CH:18]1[C:17]2[C:9](=[CH:10][C:11]3[O:15][CH2:14][O:13][C:12]=3[CH:16]=2)[C:8]2([C:22]3[C:27](=[CH:26][CH:25]=[CH:24][CH:23]=3)[N:6]([CH2:1][CH2:2][CH2:3][CH2:4][CH3:5])[C:7]2=[O:28])[CH2:20]1

Participants

5

Procedure

To a solution of 1-pentyl-6′H-spiro[indole-3,5′-naphtho[2,3-d][1,3]dioxole]-2,8′(1H,7′H)-dione (0.20 g, 0.55 mmol) in methanol (10.0 mL) was added sodium borohydride (0.03 g, 0.83 mmol). The reaction mixture was stirred at ambient temperature for 2 h and poured into of water (100 mL) and extracted with ethyl acetate (100 mL). The organic layer was washed with water, dried over sodium sulfate and filtered. The filtrate was concentrated in vacuo to dryness. The residue was subjected to flash column chromatography to afford the title compound (0.18 g, 90%) as an oil: 1H NMR (300 MHz, CDCl3) δ 7.36-7.29 (m, 1H), 7.11-6.99 (m, 3H), 6.93 (d, 1H), 5.98 (s, 1H), 5.94-5.87 (m, 2H), 5.16 (d, 1H), 3.80-3.61 (m, 2H), 2.69 (br, 1H), 2.39 (d, 1H), 1.75-1.62 (m, 2H), 1.38-1.22 (m, 4H), 0.87 (t, 3H); 13C NMR (75 MHz, CDCl3) δ 180.5, 148.9, 148.5, 143.7, 140.5, 136.9, 132.1, 128.7, 123.7, 123.3, 108.8, 105.7, 103.2, 101.5, 74.8, 59.6, 40.4, 28.9, 27.0, 22.3, 14.0; MS (ES+) m/z 388.4 (M+23).

Workup

  1. extractionextracted with ethyl acetate (100 mL)
  2. washThe organic layer was washed with water
  3. dry with materialdried over sodium sulfate
  4. filtrationfiltered
  5. concentrationThe filtrate was concentrated in vacuo to dryness

Sources & evidence

ORD record
ord-ac823700e7014c5f8d1dffff9ad219b0
Source dataset
uspto-grants-2010_04
Patent number
US07700641B2

Reaction notes

Loading…