HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706501Generated: October 27, 2026
Potassium Carbonate → N-(4-(cyclopropyl(6-methoxypyridin-3-yl)methoxy)-3-methoxybenzyl)-5-iodo-3-nitropyridin-2-amine
https://huagongshe.com/reaction/706501
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Chloro-5-iodo-3-nitropyridine | HCID 1514294 | — |
| Reactant | (4-(Cyclopropyl(6-methoxypyridin-3-yl)methoxy)-3-methoxyphenyl)methanamine | HCID 118113995 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N-(4-(cyclopropyl(6-methoxypyridin-3-yl)methoxy)-3-methoxybenzyl)-5-iodo-3-nitropyridin-2-amine | HCID 118114000 | 58.2% |
Reaction Steps
To a stirred solution of (4-(cyclopropyl(6-methoxypyridin-3-yl)methoxy)-3-methoxyphenyl)methanamine (2.50 g, 7.95 mmol) and potassium carbonate (1.41 g, 10.20 mmol) in acetonitrile (10 mL) was added 2-chloro-5-iodo-3-nitropyridine (2.90 g, 10.20 mmol). The resulting mixture was heated to 80° C. After 2 h, the mixture was filtered, and the filtrate was concentrated. Chromatographic purification of the residue (silica gel, 20% ethyl acetate in petroleum ether elute) afforded 2.60 g (58%) of N-(4-(cyclopropyl(6-methoxypyridin-3-yl)methoxy)-3-methoxybenzyl)-5-iodo-3-nitropyridin-2-amine as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09174986B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-c21ddea1c366453eade9cbb9fb2d3674 |
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| Source note | uspto-grants-2015_11 |
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