HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 2-(4-aminopiperidin-1-yl)-1,3-thiazole-5-carboxylate → Methyl 2-(4-{[(3,4-dichloro-5-cyano-1H-pyrrol-2-yl)carbonyl]amino}piperidin-1-yl)-1,3-thiazole-5-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 2-(4-aminopiperidin-1-yl)-1,3-thiazole-5-carboxylate | HCID 68579838 | — |
| Reactant | 3,4-Dichloro-5-cyano-1H-pyrrole-2-carbonyl chloride | HCID 86038333 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 2-(4-{[(3,4-dichloro-5-cyano-1H-pyrrol-2-yl)carbonyl]amino}piperidin-1-yl)-1,3-thiazole-5-carboxylate | HCID 68580069 | — |
Reaction Steps
TEA (0.06 ml, 0.5 mmol) was added to a solution of methyl 2-(4-aminopiperidin-1-yl)-1,3-thiazole-5-carboxylate (Intermediate 134, 0.1 g, 0.5 mmol)) in anhydrous THF. To this was added 3,4-dichloro-5-cyano-1H-pyrrole-2-carbonyl chloride (Intermediate 132, 0.1 g, 0.5 mmol) as a solution in anhydrous THF. After stirring 15 minutes, THF was removed. The product was partitioned with EtOAc and water. The organic portion was dried with MgSO4 and concentrated to a yellow oil. Trituration with ether followed by filtration yielded a tan solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07709503B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-cb69b010b6ec4119801c6729afda27e5 |
| Source note | uspto-grants-2010_05 |