HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080191Generated: October 30, 2026
Furfurylamine → 2-Amino-6-(furfurylamino)-N-(5-phenoxy-thiophen-2-ylmethyl)-nicotinamide
https://huagongshe.com/reaction/2080191
Participants
| Role | Name | HCID | Charge |
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| Reactant | Furfurylamine | HCID 3438 | — |
| Reactant | A-101 | HCID 188218 | — |
| Reactant | 2-aminochloro-N-(5-phenoxy-thiophen-2-ylmethyl)-nicotinamide | HCID 23130498 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Diisopropylethylamine | HCID 81531 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 2-Amino-6-(furfurylamino)-N-(5-phenoxy-thiophen-2-ylmethyl)-nicotinamide | HCID 23130598 | 68% |
Reaction Steps
2-Amino-6-chloro-N-(5-phenoxy-thiophen-2-ylmethyl)-nicotinamide described in Example A-101 (180 mg, 0.5 mmol) was dissolved in a mixture solution of dimethylsulfoxide (2 mL) and diisopropylethylamine (1 mL), furfurylamine (0.663 mL, 7.5 mmol) was added, and the solution was heated in a sealed tube for 13 hours 30 minutes (oil bath temperature: 135° C.). The reaction mixture was allowed to room temperature, poured into brine, and the solution was extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, then concentrated, the obtained residue was purified by NH silica gel column chromatography (ethyl acetate:hexane=2:1), and the title compound (144 mg, 0.34 mmol, 68%) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07932272B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-08831688426e44ab9c30259721c4a998 |
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| Source note | uspto-grants-2011_04 |
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