HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352018Generated: October 29, 2026
Phosphorus oxychloride → 4-Chloro-2-(ethoxymethyl)-1-(2-methylpropyl)-6-methyl-1H-imidazo[4,5-c]pyridine
https://huagongshe.com/reaction/352018
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 22715001 | HCID 22715001 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-Chloro-2-(ethoxymethyl)-1-(2-methylpropyl)-6-methyl-1H-imidazo[4,5-c]pyridine | HCID 22715004 | — |
Reaction Steps
N-[2-Chloro-4-(2-methylpropylamino)-6-methylpyridin-3-yl]-2-ethoxyacetamide (3.64 g), anhydrous toluene (100 ml), and phosphorus oxychloride (10.2 ml) were combined in a sealed glass tube and heated to 135° C. for 16 hours. The resulting reaction mixture was cooled, and the phosphorus oxychloride and toluene were removed under reduced pressure. The resulting black oil was dissolved in ethyl acetate, and the resulting solution was washed with saturated aqueous sodium bicarbonate. The basic aqueous layer was then washed with ethyl acetate. The organic layers were combined and concentrated to a black oil under reduced pressure. The oil was put through a column of silica gel using 60/40 ethyl acetate/hexane. The resulting eluted solution was dried under reduced pressure to a brown oil, which solidified after sitting for 48 hours. NMR analysis of the resulting product (2.59 g) indicated only minor impurities, and the product was carried on to the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06743920B2 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-8579ec6ebef345489bc0dd23ad52e1d7 |
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| Source note | uspto-grants-2004_06 |
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