Dimethyl Sulfate → HCID 14666748, compound

HRID 1087569Notes

Reaction equation

HRID 1087569 reaction equation
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[CH:14]=[CH:13][N:12]3[C:7](=[C:8]([C:22]([N:24]4[CH2:28][CH2:27][CH2:26][C@@H:25]4[CH2:29][OH:30])=[O:23])[CH:9]=[C:10]([C:16]4[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=4)[C:11]3=[O:15])[C:6]=2[CH:31]=1.[OH-].[Na+].S(OC)(O[CH3:38])(=O)=O>[I-].C([N+](CCCC)(CCCC)CCCC)CCC.C(Cl)Cl.O>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[CH:14]=[CH:13][N:12]3[C:7](=[C:8]([C:22]([N:24]4[CH2:28][CH2:27][CH2:26][C@@H:25]4[CH2:29][O:30][CH3:38])=[O:23])[CH:9]=[C:10]([C:16]4[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=4)[C:11]3=[O:15])[C:6]=2[CH:31]=1

Participants

7

Procedure

432 mg of (R)-1-[(10-chloro-4-oxo-3-phenyl-4H-benzo[a]quinolizin-1-yl)carbonyl]-2-pyrrolidinemethanol and 4 mg of tetrabutylammonium iodide in 2 ml of methylene chloride were held in an ultrasound bath for 30 minutes with 104 mg of sodium hydroxide in 0.1 ml of water. 0.19 ml of dimethyl sulfate was then added. After about 1 hour, an additional 0.19 ml of dimethyl sulfate was added and the mixture was allowed to react for an additional 90 minutes. The mixture was diluted with methylene chloride, washed with water, dried over sodium sulfate, filtered and evaporated. The residue was chromatographed on silica gel and the product was recrystallized from cyclohexane/ethanol. There was obtained (R)-1-[(10-chloro-4-oxo-3-phenyl-4H -benzo[a]quinolizin-1-yl)carbonyl]-2-methoxymethylpyrrolidine as yellow crystals of m.p. 137°-140°.

Workup

  1. customto react for an additional 90 minutes
  2. washwashed with water
  3. dry with materialdried over sodium sulfate
  4. filtrationfiltered
  5. customevaporated
  6. customThe residue was chromatographed on silica gel
  7. customthe product was recrystallized from cyclohexane/ethanol

Sources & evidence

ORD record
ord-e6d4695f7bf04f11bc94879b37a06ca1
Source dataset
uspto-grants-1991_07
Patent number
US05036066

Reaction notes

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