Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 5-(4-Amino-2-cyanophenyl)-1-methyl-1H-pyrrole-2-carbonitrile | HCID 16050529 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 16051278 | HCID 16051278 | 33% |
Reaction Steps
A mixture of methanesulfonyl chloride (0.074 mL, 1 mmol) and 5-(4-amino-2-cyanophenyl)-1-methyl-1H-pyrrole-2-carbonitrile (0.166 g, 0.75 mmol) in pyridine (1 mL) was heated to 50° C. for 4 hours. The reaction mixture was acidified with 1N HCl solution and extracted with ethyl acetate. The combined organic layers were dried over magnesium sulfate and concentrated. The residue was purified by silica gel column chromatography (hexane/ethylacetate, 90/10 to 60/40) to afford the title compound (0.059 g, 33%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07291643B2 |
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| Source dataset | uspto-grants-2007_11 |
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| ORD ID | ord-857aa4ff201a4ba2b8a6a7efa3692b48 |
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| Source note | uspto-grants-2007_11 |
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