HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1984604Generated: November 1, 2026
2,9-Dimethyl-1,10-phenanthroline → 2-Amino-5-[4-(piperidine-1-sulfonyl)-phenylsulfanyl]-isonicotinic acid pentyl ester
https://huagongshe.com/reaction/1984604
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,9-Dimethyl-1,10-phenanthroline | HCID 65237 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | HCID 57718193 | HCID 57718193 | — |
| Reactant | 4-(N-piperidinylsulfonyl)thiophenol | HCID 57718290 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Amino-5-[4-(piperidine-1-sulfonyl)-phenylsulfanyl]-isonicotinic acid pentyl ester | HCID 57718213 | 56% |
Reaction Steps
Copper iodide (26 mg, 0.14 mmol) and neocuproine (29 mg, 0.14 mmol) were added to a stirred mixture of 2-amino-5-iodo-isonicotinic acid pentyl ester (450 mg, 1.35 mmol), 4-(piperidine-1-sulfonyl)-benzenethiol (449 mg, 1.49 mmol) and sodium t-butoxide (195 mg, 2.025 mmol) in toluene (10 ml) and the reaction was heated to reflux overnight. The reaction was cooled to room temperature, solids filtered off through celite and the filtrate concentrated under reduced pressure onto silica. The residue was purified by flash column chromatography using ethyl acetate 2/3 hexane as eluent to afford 2-amino-5-[4-(piperidine-1-sulfonyl)-phenylsulfanyl]-isonicotinic acid pentyl ester as an orange solid (348 mg, 56%). 1H NMR (CDCl3): (1H, s, py); 7.51 (2H, d, Ar); 7.10 (2H, d, Ar); 6.80 (1H, s, py); 4.92 (2H, br s, NH2); 4.14 (2H, t, OCH2); 2.90 (4H, m, 2×CH2N pip); 1.53 (6H, m, OCH2CH2, 2×CH2 pip); 1.46 (2H, m, CH2 pip); 1.24 (4H, m, OCH2CH2CH2CH2CH3); 0.80 (3H, t, CH2CH3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07544702B2 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-8e1046b6e9b44611a5aae62713ac15c6 |
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| Source note | uspto-grants-2009_06 |
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