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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204359Generated: October 30, 2026

5-Chloro-2-methylaniline → Methyl 5-bromo-2-(((5-chloro-2-methylphenyl)amino)(5-chloropyridin-2-yl)methyl)-1-isopropyl-1H-pyrrole-3-carboxylate

https://huagongshe.com/reaction/2204359

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloro-2-methylanilineHCID 7260—
Reactant2-[(4-chloro-phenyl)-hydroxy-methyl]-1-isopropyl-1H-pyrrole-3-carboxylic acid ethyl esterHCID 86703105—
Reactant3-Amino-5-chloro-1-methylpyridin-2(1H)-oneHCID 86703118—
Reactant5-bromo-2-[(5-chloro-pyridin-2-yl)-hydroxy-methyl]-1-isopropyl-1H-pyrrole-3-carboxylic acid methyl esterHCID 86703161—
ProductMethyl 5-bromo-2-(((5-chloro-2-methylphenyl)amino)(5-chloropyridin-2-yl)methyl)-1-isopropyl-1H-pyrrole-3-carboxylateHCID 86703168—

Reaction Steps

The title compound was prepared in analogy to the procedure described for Step L3 but 5-bromo-2-[(5-chloro-pyridin-2-yl)-hydroxy-methyl]-1-isopropyl-1H-pyrrole-3-carboxylic acid methyl ester (Step BK2) and 5-chloro-2-methyl-phenylamine were used instead of 2-[(4-chloro-phenyl)-hydroxy-methyl]-1-isopropyl-1H-pyrrole-3-carboxylic acid ethyl ester and 3-amino-5-chloro-1-methyl-1H-pyridin-2-one respectively. The title compound was obtained as a yellow-brown solid. ESI-MS: tR=1.59 min, [M+H]+ 510/512/514 (LC-MS 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365576B2
Source datasetuspto-grants-2016_06
ORD IDord-b6291bee877d4b2cab3a00a596587670
Source noteuspto-grants-2016_06