HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 178513548, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethanesulfonylchloride, 2-chloro- | HCID 15385 | — |
| Reactant | Piperidin-4-ol | HCID 79341 | — |
| Reactant | 5-(3-fluorophenyl)-3-(4-piperidinyl)-1H-indazole-7-carboxamide | HCID 178513539 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178513548 | HCID 178513548 | 20.2% |
Reaction Steps
The title compound was prepared according to the procedure described in Example 33. Thus, 5-(3-fluorophenyl)-3-(4-piperidinyl)-1H-indazole-7-carboxamide (Intermediate 15) (75 mg, 0.167 mmol) was reacted with 2-chloro-1-ethanesulfonyl chloride (17 uL, 0.167 mmol) in the presence of triethyl amine (93 uL, 0.665 mmol) in DMF (2 mL) at 0° C. After 10 mins., K2CO3 (46 mg, 0.334 mmol) and 4-piperidinol (51 mg, 0.501 mmol) were added to afford the title compound (17.9 mg, 20% for 2 steps).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08501780B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-d340445d90284b1b8da3caccc3f5c0db |
| Source note | uspto-grants-2013_08 |