Indole-5-carboxaldehyde → HCID 86598195, compound

HRID 900786Notes

Reaction equation

HRID 900786 reaction equation
C[O-].[Na+].[Na].[NH:5]1[C:13]2[C:8](=[CH:9][C:10]([CH:14]=O)=[CH:11][CH:12]=2)[CH:7]=[CH:6]1.[N:16]([CH2:19][C:20]([O:22][CH3:23])=[O:21])=[N+:17]=[N-:18]>O.CO>[N:16](/[C:19](=[CH:14]\[C:10]1[CH:9]=[C:8]2[C:13](=[CH:12][CH:11]=1)[NH:5][CH:6]=[CH:7]2)/[C:20]([O:22][CH3:23])=[O:21])=[N+:17]=[N-:18]

Participants

7

Procedure

Under nitrogen, to a sodium methoxide solution (prepared from 15 ml of methanol and 0.66 g (29 mmol) of sodium) a mixture of 1.02 g (7 mmol) of indole-5-carbaldehyde [Helv. Chim. Acta, 1616. (1968)], 3.34 g (29 mmol) of methyl azido-acetate and 7 ml of methanol is added dropwise at 0° C. and the so obtained mixture is stirred at this temperature for 5 h. Then the reaction mixture is diluted with 50 ml of water, and extracted three times with 50 ml of chloroform. The combined organic layers are washed with 20 ml of water, filtered through a phase separating filter-paper and concentrated to yield 1.3 g (77%) of the title compound. Mp.: 130-133° C. (chloroform).

Workup

  1. additionis added dropwise at 0° C.
  2. extractionextracted three times with 50 ml of chloroform
  3. washThe combined organic layers are washed with 20 ml of water
  4. filtrationfiltered through a phase
  5. customseparating
  6. filtrationfilter-paper
  7. concentrationconcentrated

Sources & evidence

ORD record
ord-fbcdb68293d443a5b1f25e22b83451c4
Source dataset
uspto-grants-2008_04
Patent number
US07361670B2

Reaction notes

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