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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 506196Generated: November 1, 2026

HCID 68467005, compound → HCID 44626360, compound

https://huagongshe.com/reaction/506196

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68467005HCID 68467005—
SolventTrifluoroacetic acid methylene chlorideHCID 21863450—
ProductHCID 44626360HCID 4462636090.4%

Reaction Steps

A mixture of tert-butyl 4-[(2-{5-cyano-4-[(4-methyl-1H-indol-5-yl)amino]pyridin-3-yl}-1-benzofuran-5-yl)methyl]piperazine-1-carboxylate (63 mg, 0.11 mmol) in 10% trifluoroacetic acid/CH2Cl2 was stirred at room temperature for 4 h, concentrated in vacuo, and the residue was purified by preparative HPLC (column: Prodigy ODS3, 4.6×150 mm, from Phenomenex (Torrance, Calif.); mobile phase A: 0.02% trifluoroacetic acid (TFA) in water; mobile phase B: 0.02% TFA in CH3CN, 10-95% B in 25 minutes (min.); flow rate: 1.0 mL/min; column temperature: 40° C.; detection wavelength: 254 and 215 nm) to provide 46 mg (50%) of the trifluoroacetic salt of 4-[(4-methyl-1H-indol-5-yl)amino]-5-[5-(piperazin-1-ylmethyl)-1-benzofuran-2-yl]nicotinonitrile 540 as an orange solid. HPLC retention time: 5.8 min.(g); MS: 463.3 (M+H); melting point: 113-115° C.; and HRMS: 463.2234.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781591B2
Source datasetuspto-grants-2010_08
ORD IDord-c857581ebf8940b181ce9ceb8e197c60
Source noteuspto-grants-2010_08