HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1267724Generated: November 1, 2026
2-Amino-5-methylpyridine → HCID 69539502, compound
https://huagongshe.com/reaction/1267724
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Amino-5-methylpyridine | HCID 15348 | — |
| Reactant | HCID 86758935 | HCID 86758935 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 69539502 | HCID 69539502 | 16% |
Reaction Steps
A mixture of (R)-N-(2,3-dichloro-4-chlorosulphonylphenyl)-3,3,3-trifluoro-2-hydroxy-2-methylpropanamide (200 mg, 0.5 mmol) (Method 1) and 2-amino-5-methylpyridine (81 mg, 0.80 mmol) in pyridine (5 ml) was stirred at 80° C. overnight. The mixture was cooled to ambient temperature, poured onto water (50 ml) and extracted with EtOAc (2×25 ml). The organic layer was separated, washed with 1 M aqueous hydrochloric acid, saturated sodium hydrogen carbonate solution, brine, dried and evaporated to give the title compound as a solid (40 mg, 0.08 mmol); NMR: 1.6 (s, 3H), 2.1 (s, 3H), 7.1 (d, 1H), 7.6 (d, 1H), 7.75 (s, 1H), 8.1 (s, 2H); m/z 470.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06552225B1 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-86db82e5db1f473dbbfc2ef38443447b |
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| Source note | uspto-grants-2003_04 |
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