Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ethyl isothiocyanatoformate | HCID 85320 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | HCID 67068467 | HCID 67068467 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11594627 | HCID 11594627 | 15.3% |
Reaction Steps
Ethoxycarbonyl isothiocyanate (0.12 g, 0.90 mmol) was added to 3-[(6-ethoxy-pyridin-2-ylmethyl)-amino]-1H-pyrrole-2-carboxylic acid ethyl ester (0.24 g, 0.82 mmol) in CH2Cl2 (5 mL) and the solution was stirred at ambient temperature for 35 minutes. The solvent was evaporated and 0.4M NaOEt in ethanol (3 mL, 1.2 mmol) was added to the residue and the mixture was refluxed for 1 h. More NaOEt (0.4M in ethanol, 1.5 mL, 0.6 mmol) was added and the solution was refluxed for another 1.5 h. The solvent was evaporated, the residue was dissolved in water and the pH adjusted to neutral pH with 1M HCl. The resulting solid was collected, washed, and dried to give crude product. This material was purified by preparative HPLC to yield the title compound (38 mg, 15%) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08859568B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-312a073801954911b89b8e8f0e71c7de |
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| Source note | uspto-grants-2014_10 |
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