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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 506205Generated: November 1, 2026

tert-butyl 4-[(2-{4-[(7-chloro-4-methyl-1H-indol-5-yl)amino]-5-cyanopyridin-3-yl}-1-benzofuran-5-yl)methyl]piperazine-1-carboxylate → 4-[(7-chloro-4-methyl-1H-indol-5-yl)amino]-5-[5-(piperazin-1-ylmethyl)-1-benzofuran-2-yl]nicotinonitrile

https://huagongshe.com/reaction/506205

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl 4-[(2-{4-[(7-chloro-4-methyl-1H-indol-5-yl)amino]-5-cyanopyridin-3-yl}-1-benzofuran-5-yl)methyl]piperazine-1-carboxylateHCID 68463392—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acidHCID 6422—
Product4-[(7-chloro-4-methyl-1H-indol-5-yl)amino]-5-[5-(piperazin-1-ylmethyl)-1-benzofuran-2-yl]nicotinonitrileHCID 68465800—

Reaction Steps

A solution of tert-butyl 4-[(2-{4-[(7-chloro-4-methyl-1H-indol-5-yl)amino]-5-cyanopyridin-3-yl}-1-benzofuran-5-yl)methyl]piperazine-1-carboxylate (176 mg, 0.29 mmol) in CH2Cl2 (4 mL) and trifluoroacetic acid (2 mL) was stirred at room temperature for 4 h and concentrated to provide 4-[(7-chloro-4-methyl-1H-indol-5-yl)amino]-5-[5-(piperazin-1-ylmethyl)-1-benzofuran-2-yl]nicotinonitrile as a yellow solid in quantitative yield (182 mg). HPLC retention time: 6.5 min.(g); MS: 497.3 (M+H); and HRMS: 497.1851.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781591B2
Source datasetuspto-grants-2010_08
ORD IDord-2cba2587a48e492ab5b032a41e53c4c4
Source noteuspto-grants-2010_08