Ethyl bromoacetate → HCID 21790152, compound

HRID 2164336Notes

Reaction equation

HRID 2164336 reaction equation
[CH2:1]([O:3][C:4]([C:6]1[N:7]([CH3:16])[C:8]2[C:13]([C:14]=1[OH:15])=[CH:12][CH:11]=[CH:10][CH:9]=2)=[O:5])[CH3:2].Br[CH2:18][C:19]([O:21][CH2:22][CH3:23])=[O:20]>>[CH2:1]([O:3][C:4]([C:6]1[N:7]([CH3:16])[C:8]2[C:13]([C:14]=1[O:15][CH2:18][C:19]([O:21][CH2:22][CH3:23])=[O:20])=[CH:12][CH:11]=[CH:10][CH:9]=2)=[O:5])[CH3:2]

Participants

3

Reactant 2

HCID 7748Ethyl bromoacetateHCID 54696099Ethyl 3-hydroxy-1-methyl-1H-indole-2-carboxylate

Product 1

HCID 21790152HCID 21790152, compound

Procedure

Prepared by the procedure described in Example 1 from 3-hydroxy-1-methyl-1H-indole-2-carboxylic acid ethyl ester and ethyl bromoacetate. The crude oil product obtained after evaporation was used for further synthesis without additional purification.

Workup

  1. customPrepared by the procedure
  2. customThe crude oil product obtained
  3. customafter evaporation
  4. customwas used for further synthesis without additional purification

Sources & evidence

ORD record
ord-9d1196acfee4444ca22747546903152b
Source dataset
uspto-grants-1985_03
Patent number
US04503236

Reaction notes

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