Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396506Generated: October 26, 2026

[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

https://huagongshe.com/reaction/396506

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[6-Chloro-2-(4-methylpyridine-2-Carbonyl)-1H-indol-3-yl]acetic AcidHCID 9862267—
ReactantMethyl trans-5-tert-butyl-2-(p-toluenesulfonylamino)cinnamateHCID 23003394—
ProductMethyl[5-tert-butyl-2-(4-methylpyridine-2-carbonyl)-1h-indol-3-yl]acetateHCID 23003388—

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06608070B1
Source datasetuspto-grants-2003_08
ORD IDord-1cacd61cd91143f8942e80ed351d7cdf
Source noteuspto-grants-2003_08