HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → 1,3-dimethyl-1H-thieno[2,3-c]pyrazole-5-carbonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 1,3-dimethyl-1H-thieno[2,3-c]pyrazole-5-carboxylic acid | HCID 2776541 | — |
| Reactant | HCID 11510715 | HCID 11510715 | — |
| Reactant | HCID 60136483 | HCID 60136483 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1,3-dimethyl-1H-thieno[2,3-c]pyrazole-5-carbonyl chloride | HCID 2776542 | — |
| Product | HCID 11648888 | HCID 11648888 | — |
Reaction Steps
N-(4-Chlorophenyl)-N-{(2S,4R)-1-[(1,3-dimethyl-1H-thieno[2,3-c]pyrazol-5-yl)carbonyl]-2-methyl-1,2,3,4-tetrahydroquinolin-4-yl}acetamide was prepared following the procedure for N-(4-chlorophenyl)-N-{(2S,4R)-1-[(1-isopropyl-1H-pyrazol-4-yl)carbonyl]-2-methyl-1,2,3,4-tetrahydroquinolin-4-yl}acetamide substituting 1,3-dimethyl-1H-thieno[2,3-c]pyrazole-5-carbonyl chloride for 1-isopropyl-1H-pyrazole-4-carbonyl chloride. (1,3-Dimethyl-1H-thieno[2,3-c]pyrazole-5-carbonyl chloride was prepared from commercially available 1,3-dimethyl-1H-thieno[2,3-c]pyrazole-5-carboxylic acid by treatment with oxalyl chloride and catalytic DMF in dichloromethane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07504508B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-a92fb496713c4fc5871cfb210e11746e |
| Source note | uspto-grants-2009_03 |