HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643690Generated: November 2, 2026
2-Aminopyridine → 2-Benzyl-4-isopropoxy-2,3-dihydro-benzofuran-6-carboxylic acid pyridin-2-ylamide
https://huagongshe.com/reaction/1643690
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Aminopyridine | HCID 10439 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | HCID 59560120 | HCID 59560120 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Benzyl-4-isopropoxy-2,3-dihydro-benzofuran-6-carboxylic acid pyridin-2-ylamide | HCID 59560133 | 21% |
Reaction Steps
A mixture of 2-benzyl-4-isopropoxy-2,3-dihydro-benzofuran-6-carboxylic acid (220j) (0.5 g, 1.9 mmol), DIPEA (0.37 g, 2.85 mmol) and HATU (0.74 g, 1.94 mmol) in DMF (15 mL) was stirred at room temperature for 1 hr, and then pyridin-2-amine (0.18 g, 1.94 mmol) was added in one portion. The mixture was stirred at room temperature overnight. TLC (EtOAc/petroleum ether=1/2) indicated that the reaction was complete. The mixture was concentrated. The residue was purified by prep. HPLC to give the title compound (73 mg, 21% yield, TFA salt) as a white solid. 1H NMR (400 MHz, CDCl3): δ11.71 (br, 1H), 8.76 (d, 1H), 8.27 (d, 1H), 8.14 (t, 1H), 7.17˜7.46 (m, 9H), 4.96 (d, 1H), 4.78 (t, 1H), 2.82 (m, 1H), 2.67 (m, 1H), 2.19 (m, 1H), 1.96 (m, 1H), 1.32 (d, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08119624B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-7c9090f7c20f4c2ebcbe056cac553b19 |
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| Source note | uspto-grants-2012_02 |
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