Methyl trans 5-chloro-2-(phenylsulfonylamino)cinnamate → Methyl[5-chloro-2-(4-chloropyridine-2-carbonyl)-1h-indol-3-yl]acetate

Participants

Role	Name	HCID	Charge
Reactant	Methyl trans 5-chloro-2-(phenylsulfonylamino)cinnamate	HCID 11187263	—
Reactant	2-Bromo-1-(4-chloro-pyridin-2-yl)-ethanone hydrobromide	HCID 23003349	—
Product	Methyl[5-chloro-2-(4-chloropyridine-2-carbonyl)-1h-indol-3-yl]acetate	HCID 23003461	—

Reaction Steps

The title compound was prepared according to the procedure described in Example 57 from methyl trans-5-chloro-2-(phenylsulfonylamino)cinnamate (Example 36, step 3) and 2-bromoacetyl-4-chloropyridine hydrobromide (Preparation is described in Example 33).

Provenance & Evidence

DOI	10.6084/m9.figshare.5104873.v1
Patent number	US06608070B1
Source dataset	uspto-grants-2003_08
ORD ID	ord-b36622c7fc3e48cea254b2dee64ed009
Source note	uspto-grants-2003_08