HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-[1-(ethylsulfonyl)-4-piperidinyl]-5-(2-thienyl)-1H-indazole-7-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethanesulfonyl chloride | HCID 11667 | — |
| Reactant | HCID 178479541 | HCID 178479541 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-[1-(ethylsulfonyl)-4-piperidinyl]-5-(2-thienyl)-1H-indazole-7-carboxamide | HCID 178477700 | — |
Reaction Steps
This compound was prepared in a fashion analogous to the procedure described in Example 3. Thus, 3-(4-piperidinyl)-5-(2-thienyl)-1H-indazole-7-carboxamide hydrochloride (Intermediate 17) (0.117 mmol) was reacted with ethane sulfonyl chloride (0.02 mL, 0.234 mmol) in the presence of triethylamine (0.04 mL, 0.468 mmol) in methylene chloride (10 mL) to give the title compound (4.9 mg, 10% for the last two steps)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08501780B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-5a527080ae2d432f8f8626e2f5be199b |
| Source note | uspto-grants-2013_08 |