4-Methylmorpholine → HCID 19871150, compound

HRID 329745Notes

Reaction equation

HRID 329745 reaction equation
[NH2:1][CH:2]1[CH:7]2[CH2:8][CH2:9][N:4]([CH2:5][CH2:6]2)[CH2:3]1.CN1CCOCC1.[CH3:17][N:18]1[C:23]2[CH:24]=[CH:25][CH:26]=[C:27]([C:28]([Cl:30])=[O:29])[C:22]=2[O:21][CH2:20][C:19]1=[O:31]>C(Cl)(Cl)Cl>[ClH:30].[CH3:17][N:18]1[C:23]2[CH:24]=[CH:25][CH:26]=[C:27]([C:28]([NH:1][CH:2]3[CH:7]4[CH2:8][CH2:9][N:4]([CH2:5][CH2:6]4)[CH2:3]3)=[O:29])[C:22]=2[O:21][CH2:20][C:19]1=[O:31]

Participants

5

Procedure

To a solution of 2.91 g of 3-aminoquinuclidine and 2.46 g of N-methylmorpholine in 30 ml of chloroform is added a solution of 5.0 g of 3,4-dihydro-4-methyl-3-oxo-2H-1,4-benzoxazine-8-carboxylic acid chloride in 70 ml of chloroform under cooling and stirring followed by stirring for 7 hours. The resultant solution is washed with water, aqueous sodium hydrogen carbonate and then water, and dried over magnesium sulfate. After the solvent is distilled off under reduced pressure, the residue is purified with column chromatography using chloroform as an eluent and treated with ethanolic hydrochloric acid to give 3,4-dihydro-4-methyl-3-oxo-N-(3 -quinuclidinyl)-2H-1,4-benzoxazine-8-carboxamide hydrochloride, melting at 271°-272° C. with decomposition.

Workup

  1. temperatureunder cooling
  2. stirringby stirring for 7 hours
  3. washThe resultant solution is washed with water, aqueous sodium hydrogen carbonate
  4. dry with materialwater, and dried over magnesium sulfate
  5. distillationAfter the solvent is distilled off under reduced pressure
  6. customthe residue is purified with column chromatography
  7. additiontreated with ethanolic hydrochloric acid

Sources & evidence

ORD record
ord-80084bcbd0ed49c89da702e40c718bb9
Source dataset
uspto-grants-1990_01
Patent number
US04892872

Reaction notes

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