HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1245705Generated: October 26, 2026
3-Aminopentan-2-ol → 4-(1-Ethyl-2-hydroxy-propylamino)-6-methyl-2-(2,4,6-trimethyl-phenoxy)-nicotinic acid methyl ester
https://huagongshe.com/reaction/1245705
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Aminopentan-2-ol | HCID 226832 | — |
| Reactant | 4-Chloro-2-(2,4,6-trimethyl-phenoxy)-6-methyl-nicotinic acid methyl ester | HCID 24805651 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 4-(1-Ethyl-2-hydroxy-propylamino)-6-methyl-2-(2,4,6-trimethyl-phenoxy)-nicotinic acid methyl ester | HCID 69587356 | — |
Reaction Steps
A mixture of 4-chloro-2-(2,4,6-trimethyl-phenoxy)-6-methyl-nicotinic acid methyl ester (250 mg, 0.78 mmol) and 3-amino-pentan-2-ol (320 mg, 3.13 mmol) in DMSO was heated in 130° C. oil bath for 24 hr. The mixture cooled to rt and quenched with water and extracted with ethyl acetate. The organic layer was separated, washed with water, dried over anhydrous sodium sulfate, filtered, and concentrated to dryness to give 280 mg of crude product as an oil. The oil was purified through silica gel column chromatography using 20% ethyl acetate in hexane as eluent to give the title compound as a yellow solid, mp 116–120° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07125880B1 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-6247620705644528bf6727f9d3aebd86 |
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| Source note | uspto-grants-2006_10 |
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