HuagongsheHuagongshe Chemistry Print Report · For research reference only
N,N'-Dicyclohexylurea → 4-Ethylthio-5-methyl-6-(1-ethylpyrazol-5-yl)oxycarbonyl-8-chlorothiochroman
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N,N'-Dicyclohexylurea | HCID 4277 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 4-Ethylthio-5-methyl-6-carboxy-8-chlorothiochroman | HCID 22118415 | — |
| Reactant | HCID 178418331 | HCID 178418331 | — |
| Solvent | 2-Methyl-2-butanol | HCID 6405 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-Ethylthio-5-methyl-6-(1-ethylpyrazol-5-yl)oxycarbonyl-8-chlorothiochroman | HCID 22118393 | 106.9% |
Reaction Steps
1.0 Gram (3.3 mmol) of 4-ethylthio-5-methyl-6-carboxy-8-chlorothiochroman was dissolved in 5 ml of t-amyl alcohol, and 0.45 g (4.0 mmol, 1.2 eq.) of 1-ethyl-5-hydroxypyrazole and 0.83 g (4.0 mmol, 1.2 eq.) of N,N'-dicyclohexylcarbodiimide were added. The mixture was stirred at room temperature for 2.5 hours. After the completion of the reaction, ethyl acetate and hexane were added, and liberated N,N'-dicyclohexylurea was filtered off. The filtrate was concentrated and purified by column chromatography (silica gel/hexane+ethyl acetate=5:1) to give 1.4 g (yield 100%) of 4-ethylthio-5-methyl-6-(1-ethylpyrazol-5-yl)oxycarbonyl-8-chlorothiochroman.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06159904 |
| Source dataset | uspto-grants-2000_12 |
| ORD ID | ord-705e8cc1da8d4e1f80bef8834a0e5663 |
| Source note | uspto-grants-2000_12 |