HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 18440729, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 5-Chlorothiophene-2-carbonyl Chloride | HCID 589223 | — |
| Reactant | HCID 18440731 | HCID 18440731 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18440729 | HCID 18440729 | — |
Reaction Steps
At 0° C., 0.97 g (5.35 mmol) of 5-chlorothiophene-2-carbonyl chloride is added dropwise to a suspension of 1.48 g (4.12 mmol) of tert-butyl 4-[2-(4-amino-1-oxo-1,3-dihydro-2H-isoindol-2-yl)ethyl]-1-piperidinecarboxylate, 1.7 ml (20.6 mmol) of pyridine and 25 mg (0.206 mmol) of 4-DMAP in 21 ml of absolute THF. The mixture is slowly warmed to room temperature and stirred overnight. The reaction 10 mixture is concentrated and then separated by chromatography on silica gel (dichloromethane/methanol 97:3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07189738B2 |
| Source dataset | uspto-grants-2007_03 |
| ORD ID | ord-5602b2d43d844785849e684ca57a4a8e |
| Source note | uspto-grants-2007_03 |