Nitric Acid → HCID 131716240、化合物

HRID 329746

反応式

HRID 329746 の反応式
[Cl:1][C:2]1[CH:3]=[C:4]([C:14]([NH:16][CH:17]2[CH:22]3[CH2:23][CH2:24]N(CC3)C2)=[O:15])[C:5]2[O:10][CH2:9][C:8](=[O:11])[N:7]([CH3:12])[C:6]=2[CH:13]=1.[N+:25]([O-:28])(O)=[O:26]>S(=O)(=O)(O)O>[OH2:10].[ClH:1].[Cl:1][C:2]1[C:3]([N+:25]([O-:28])=[O:26])=[C:4]([C:14]([NH:16][CH:17]2[CH2:22][CH:23]3[CH2:24][CH2:8][N:7]2[CH2:6][CH2:5]3)=[O:15])[C:5]2[O:10][CH2:9][C:8](=[O:11])[N:7]([CH3:12])[C:6]=2[CH:13]=1.[Cl:1][C:2]1[C:3]([N+:25]([O-:28])=[O:26])=[C:4]([C:14]([NH:16][CH:17]2[CH2:22][CH:23]3[CH2:24][CH2:17][N:16]2[CH2:14][CH2:4]3)=[O:15])[C:5]2[O:10][CH2:9][C:8](=[O:11])[N:7]([CH3:12])[C:6]=2[CH:13]=1.[ClH:1]

参加物

4

実験手順

A solution of 10.5 g of 6-chloro-3,4-dihydro-4-methyl-3-oxo-N-(3-quinuclidinyl)-2H-1,4-benzoxazine-8-carboxamide in 50 ml of concentrated sulfuric acid is cooled to a temperature below 0° C., and a mixture of 1.5 ml of fuming nitric acid (d 1.50) and 1.5 ml of concentrated sulfuric acid is added dropwise thereto at a temperature below 5° C. The resultant mixture is stirred under ice-cooling for 1.5 hours and poured into ice-cold water. After extracting with ethyl acetate, the extract is washed with water and dried over magnesium sulfate. The solvent is distilled off followed by recrystallizing from ethanol and treating with ethanolic hydrochloric acid to give 6-chloro-3,4-dihydro-4-methyl-7-nitro-3-oxo-N-(quinuclidinyl)-2H-1,4-benzoxazine-8-carboxamide hydrochloride hemihydrate. The melting point and NMR spectra are identical with those of the compound as prepared in Example 30(1).

後処理

  1. additionis added dropwise
  2. customat a temperature below 5° C
  3. temperaturecooling for 1.5 hours
  4. additionpoured into ice-cold water
  5. extractionAfter extracting with ethyl acetate
  6. washthe extract is washed with water
  7. dry with materialdried over magnesium sulfate
  8. distillationThe solvent is distilled off
  9. customby recrystallizing from ethanol
  10. additiontreating with ethanolic hydrochloric acid

出典と根拠

ORDレコード
ord-ef1278346bae4fbfafd5f107b4b3da05
出典データセット
uspto-grants-1990_01
特許番号
US04892872

関連ノート

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