[6-Chloro-2-(4-methylpyridine-2-Carbonyl)-1H-indol-3-yl]acetic Acid → Methyl[5-tert-butyl-2-(4-methylpyridine-2-carbonyl)-1h-indol-3-yl]acetate

HRID 396506Notes

Reaction equation

HRID 396506 reaction equation
[C:1]([C:5]1[CH:6]=[CH:7][C:8]([NH:17]S(C2C=CC(C)=CC=2)(=O)=O)=[C:9]([CH:16]=1)/[CH:10]=[CH:11]/[C:12]([O:14][CH3:15])=[O:13])([CH3:4])([CH3:3])[CH3:2].ClC1C=C2C(C(CC(O)=O)=[C:34]([C:38]([C:40]3[CH:45]=[C:44]([CH3:46])[CH:43]=[CH:42][N:41]=3)=[O:39])N2)=CC=1>>[CH3:15][O:14][C:12](=[O:13])[CH2:11][C:10]1[C:9]2[C:8](=[CH:7][CH:6]=[C:5]([C:1]([CH3:2])([CH3:3])[CH3:4])[CH:16]=2)[NH:17][C:34]=1[C:38]([C:40]1[CH:45]=[C:44]([CH3:46])[CH:43]=[CH:42][N:41]=1)=[O:39]

Participants

3

Reactant 2

HCID 9862267[6-Chloro-2-(4-methylpyridine-2-Carbonyl)-1H-indol-3-yl]acetic AcidHCID 23003394Methyl trans-5-tert-butyl-2-(p-toluenesulfonylamino)cinnamate

Product 1

HCID 23003388Methyl[5-tert-butyl-2-(4-methylpyridine-2-carbonyl)-1h-indol-3-yl]acetate

Procedure

The compound was prepared according to the procedure described in Example of 57 from methyl trans-5-tert-butyl-2-(p-toluenesulfonylamino)cinnamate (step 2) and 2-bromoacetyl-4-methylpyridine hydrobromide (Preparation is described in step 2 of Example 31).

Workup

  1. customThe compound was prepared

Sources & evidence

ORD record
ord-1cacd61cd91143f8942e80ed351d7cdf
Source dataset
uspto-grants-2003_08
Patent number
US06608070B1

Reaction notes

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