Hydrochloric Acid → HCID 21938236, compound

HRID 1242144Notes

Reaction equation

HRID 1242144 reaction equation
[Cl:1][C:2]1[CH:23]=[C:22]([Cl:24])[CH:21]=[CH:20][C:3]=1[C:4]([C:6]1[NH:7][C:8]2[C:13]([C:14]=1[CH3:15])=[CH:12][CH:11]=[C:10]([C:16]([O:18]C)=[O:17])[CH:9]=2)=O.O.NN.[OH-].[K+].Cl>C(O)CO.O>[C:16]([C:10]1[CH:9]=[C:8]2[C:13]([C:14]([CH3:15])=[C:6]([CH2:4][C:3]3[CH:20]=[CH:21][C:22]([Cl:24])=[CH:23][C:2]=3[Cl:1])[NH:7]2)=[CH:12][CH:11]=1)([OH:18])=[O:17]

Participants

7

Conditions

Temperature
160 °C

Procedure

2-(2,4-Dichlorobenzoyl)-6-(methoxycarbonyl)-3-methylindole (1.00 g) is suspended in ethylene glycol (10 ml), to which is added hydrazine monohydrate (0.83 g), and stirred under heat at 160° C. for 3 hours. After this is once cooled, potassium hydroxide (1.1 g) is added thereto, and again stirred under heat at 155° C. for 3 hours. After cooled, the reaction mixture is made acidic with water and 1 M HCl added thereto. Then, this is extracted with ethyl acetate. The organic layer is washed with a saturated saline solution, and dried with anhydrous sodium sulfate. Then, the drying agent is removed through filtration, and the filtrate is concentrated under reduced pressure. The resulting crystalline residue is washed with a mixed solution of ethyl acetate and hexane, and dried to obtain 6-carboxy-2-(2,4-dichlorobenzyl)-3-methylindole (86) (0.63 g).

Workup

  1. temperatureAfter this is once cooled
  2. stirringagain stirred
  3. temperatureunder heat at 155° C. for 3 hours
  4. temperatureAfter cooled
  5. additionadded
  6. extractionThen, this is extracted with ethyl acetate
  7. washThe organic layer is washed with a saturated saline solution
  8. dry with materialdried with anhydrous sodium sulfate
  9. customThen, the drying agent is removed through filtration
  10. concentrationthe filtrate is concentrated under reduced pressure
  11. washThe resulting crystalline residue is washed with a mixed solution of ethyl acetate and hexane
  12. customdried

Sources & evidence

ORD record
ord-f82cb5884c8d45f6a9b7557c6965adb9
Source dataset
uspto-grants-2006_10
Patent number
US07115647B2

Reaction notes

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