Hydrochloric Acid → HCID 86720822, compound

HRID 877322Notes

Reaction equation

HRID 877322 reaction equation
[C:1]1([C@H:7]([NH:37][C:38]([O:40][C@@H:41]2[CH:46]3[CH2:47][CH2:48][N:43]([CH2:44][CH2:45]3)[CH2:42]2)=[O:39])[C:8]2[CH:9]=[C:10]([CH:34]=[CH:35][CH:36]=2)[O:11][CH2:12][C:13]2[CH:33]=[CH:32][C:16]([C:17]([O:19][CH2:20][C:21]3[CH:26]=[CH:25][CH:24]=[C:23]([CH:27]4OCC[O:28]4)[CH:22]=3)=[O:18])=[CH:15][CH:14]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.Cl>C1COCC1.C(OCC)(=O)C>[C:1]1([C@H:7]([NH:37][C:38]([O:40][C@@H:41]2[CH:46]3[CH2:47][CH2:48][N:43]([CH2:44][CH2:45]3)[CH2:42]2)=[O:39])[C:8]2[CH:9]=[C:10]([CH:34]=[CH:35][CH:36]=2)[O:11][CH2:12][C:13]2[CH:33]=[CH:32][C:16]([C:17]([O:19][CH2:20][C:21]3[CH:26]=[CH:25][CH:24]=[C:23]([CH:27]=[O:28])[CH:22]=3)=[O:18])=[CH:15][CH:14]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

Participants

5

Procedure

To a stirred solution of 3-(1,3-dioxolan-2-yl)benzyl 4-((3-((S)-phenyl((((R)-quinuclidin-3-yloxy)carbonyl)amino)methyl)phenoxy)methyl)benzoate (0.32 g, 0.57 mmol) in THF (8 mL) was added 2M aqueous hydrochloric acid (8 mL). The reaction mixture was stirred at RT for 1 hour. The mixture was diluted with ethyl acetate and was washed sequentially with saturated aqueous sodium hydrogen carbonate and brine. The organic extract was dried (magnesium sulfate), filtered and the solvent evaporated at reduced pressure. The residue was used in the next step with no further purification.

Workup

  1. washwas washed sequentially with saturated aqueous sodium hydrogen carbonate and brine
  2. extractionThe organic extract
  3. dry with materialwas dried (magnesium sulfate)
  4. filtrationfiltered
  5. customthe solvent evaporated at reduced pressure
  6. customThe residue was used in the next step with no further purification

Sources & evidence

ORD record
ord-1be0ef0861a1461d9135e20026f7ff91
Source dataset
uspto-grants-2015_03
Patent number
US08987299B2

Reaction notes

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