Hydrochloric Acid → HCID 57235519, compound

HRID 1461453Notes

Reaction equation

HRID 1461453 reaction equation
[Cl:1][C:2]1[CH:31]=[CH:30][C:5]([C:6]([N:8]2[C:16]3[C:11](=[CH:12][C:13]([O:17][CH3:18])=[CH:14][CH:15]=3)[C:10]([C:19](=[N:21][O:22]C3CCCCO3)[CH3:20])=[C:9]2[CH3:29])=[O:7])=[CH:4][CH:3]=1.Cl.[OH-].[NH4+]>O1CCCC1>[Cl:1][C:2]1[CH:31]=[CH:30][C:5]([C:6]([N:8]2[C:16]3[C:11](=[CH:12][C:13]([O:17][CH3:18])=[CH:14][CH:15]=3)[C:10]([C:19](=[N:21][OH:22])[CH3:20])=[C:9]2[CH3:29])=[O:7])=[CH:4][CH:3]=1

Participants

5

Procedure

To a solution of 1-(4-chlorobenzoyl)-5-methoxy-2-methyl -3-[1-[[(tetrahydro-2H-pyran-2-yl)oxy]imino]ethyl]-lH-indole (5.0 g, 11.3 mmol) in tetrahydrofuran (115 ml) is added 10 ml of concentrated hydrochloric acid. The reaction mixture is stirred for 21/2 hours, at which time it is neutralized with concentrated ammonium hydroxide. It is concentrated to near dryness, diluted with ethyl acetate and washed twice with water and once with a saturated solution of sodium chloride. The organic phase is further dried over magnesium sulfate, filtered, and concentrated slowly in vacuo to 50 ml. The powdery crystals are collected to give 2.8 g (70.4%) of pure 1-(4-chlorobenzoyl)-3-[1-(hydroxyimino)ethyl]-5-methoxy-2-methyl-lH-indole; mp darkens (chars) at 170°-197° C. (dec).

Workup

  1. concentrationIt is concentrated
  2. additiondiluted with ethyl acetate
  3. washwashed twice with water and once with a saturated solution of sodium chloride
  4. dry with materialThe organic phase is further dried over magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated slowly in vacuo to 50 ml
  7. customThe powdery crystals are collected

Sources & evidence

ORD record
ord-5418a4b596b141e5ad03658dabb5d6bb
Source dataset
uspto-grants-1991_12
Patent number
US05075330

Reaction notes

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