Sodium borohydride → HCID 49806334, compound

HRID 2381214Notes

Reaction equation

HRID 2381214 reaction equation
[CH2:1]([C:3]1([CH2:29][CH3:30])[N:12]2[CH2:13][CH2:14][C:15]3[C:20]([C:11]2=[C:10]([CH3:24])[C:9]2[CH:8]=[CH:7][C:6]([O:25][CH3:26])=[C:5]([O:27][CH3:28])[C:4]1=2)=[CH:19][C:18]1[O:21][CH2:22][O:23][C:17]=1[CH:16]=3)[CH3:2].[BH4-].[Na+]>CO>[CH2:29]([C:3]1([CH2:1][CH3:2])[N:12]2[CH2:13][CH2:14][C:15]3[C:20]([CH:11]2[CH:10]([CH3:24])[C:9]2[CH:8]=[CH:7][C:6]([O:25][CH3:26])=[C:5]([O:27][CH3:28])[C:4]1=2)=[CH:19][C:18]1[O:21][CH2:22][O:23][C:17]=1[CH:16]=3)[CH3:30]

Participants

4

Reactant 2

HCID 4311764Sodium borohydrideHCID 49806216HCID 49806216, compound

Product 1

HCID 49806334HCID 49806334, compoundYield 42%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Conditions

Temperature
0 °C

Procedure

To a solution of 8,8-diethyl-9,10-dimethoxy-13-methyl-5,8-dihydro-6H-[1,3]dioxolo[4,5-g]isoquino[3,2-a]isoquinoline (100 mg, 0.25 mmol) in methanol (10 mL) was added sodium borohydride (23 mg, 0.61 mmol) in small portions at 0° C. After stirring at 0° C. for 2 h, the mixture was concentrated in vacuo. The resulting residue was extracted with diethyl ether (2×50 mL), washed with water (2×25 mL), dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was re-crystallized from methanol to afford 8,8-diethyl-9,10-dimethoxy-13-methyl-5,8,13,13a-tetrahydro-6H-[1,3]dioxolo[4,5-g]isoquino[3,2-a]isoquinoline (43 mg, 42%). LC/MS m/e calcd for C25H31NO4 (M+H)+: 410.53, observed: 410.2; 1H NMR (400 MHz, DMSO-d6) δ ppm 0.48 (t, J=7.33 Hz, 3 H) 0.75 (d, J=6.82 Hz, 3 H) 0.85 (t, J=7.58 Hz, 3 H) 1.77-1.89 (m, 1 H) 1.94-2.06 (m, 1 H) 2.10-2.22 (m, 1 H) 2.23-2.36 (m, 1 H) 2.53-2.63 (m, 1 H) 2.64-2.74 (m, 1 H) 3.02 (dd, J=6.69, 2.91 Hz, 1 H) 3.16-3.26 (m, 1 H) 3.74 (s, 3 H) 3.80 (s, 3 H) 4.52 (s, 1 H) 5.94 (d, J=6.32 Hz, 2 H) 6.66 (s, 1 H) 6.79 (s, 1 H) 6.85 (d, J=8.59 Hz, 1 H) 6.96 (d, J=8.34 Hz, 1 H).

Workup

  1. concentrationthe mixture was concentrated in vacuo
  2. extractionThe resulting residue was extracted with diethyl ether (2×50 mL)
  3. washwashed with water (2×25 mL)
  4. dry with materialdried over anhydrous sodium sulfate
  5. concentrationconcentrated in vacuo
  6. customThe residue was re-crystallized from methanol

Sources & evidence

ORD record
ord-cb55875c354f4502b4040d640cfaaa3d
Source dataset
uspto-grants-2012_09
Patent number
US08258149B2

Reaction notes

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