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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1785950Generated: October 29, 2026

Oxalyl chloride → 1,3-dimethyl-1H-thieno[2,3-c]pyrazole-5-carbonyl chloride

https://huagongshe.com/reaction/1785950

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant1,3-dimethyl-1H-thieno[2,3-c]pyrazole-5-carboxylic acidHCID 2776541—
ReactantHCID 11510715HCID 11510715—
ReactantHCID 60136483HCID 60136483—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product1,3-dimethyl-1H-thieno[2,3-c]pyrazole-5-carbonyl chlorideHCID 2776542—
ProductHCID 11648888HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504508B2
Source datasetuspto-grants-2009_03
ORD IDord-a92fb496713c4fc5871cfb210e11746e
Source noteuspto-grants-2009_03