HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 506196Generated: November 1, 2026
HCID 68467005, compound → HCID 44626360, compound
https://huagongshe.com/reaction/506196
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 68467005 | HCID 68467005 | — |
| Solvent | Trifluoroacetic acid methylene chloride | HCID 21863450 | — |
| Product | HCID 44626360 | HCID 44626360 | 90.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07781591B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-c857581ebf8940b181ce9ceb8e197c60 |
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| Source note | uspto-grants-2010_08 |
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