HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12920Generated: October 29, 2026
Hydrochloric Acid → HCID 58972820, compound
https://huagongshe.com/reaction/12920
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tert-Butyl nitrite | HCID 10906 | — |
| Reactant | HCID 58972839 | HCID 58972839 | — |
| Reactant | 3-amino-1-cyclobutyl-1H-pyrazole-4-carboxylic acid ethyl ester | HCID 58972876 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 58972820 | HCID 58972820 | — |
Reaction Steps
To a mixture of tert-butyl nitrite (5.1 mL, 38.7 mmol), cuprous chloride (3.8 g, 38.7 mmol), and anhydrous acetonitrile (100 mL) was added a mixture of 5-amino-1-cyclobutyl-1H-pyrazole-4-carboxylic acid ethyl ester and 3-amino-1-cyclobutyl-1H-pyrazole-4-carboxylic acid ethyl ester (from last step without further purification) in anhydrous acetonitrile (50 mL) at 0° C. The reaction mixture was stirred at room temperature for 1 h and then at 60° C. for 2 h. The mixture was cooled to room temperature and then poured into 6N HCl (50 mL) and extracted with dichloromethane. The aqueous layer was extracted three times with dichloromethane. After the combined organic layers were concentrated in vacuo, the crude residue was purified by flash chromatography eluting with a gradient of 10-20% ethyl acetate/hexanes, then 20% ethyl acetate/hexanes. The desired fractions were concentrated in vacuo and dried under vacuum to give 5-chloro-1-cyclobutyl-1H-pyrazole-4-carboxylic acid ethyl ester (eluted first, 610 mg, 10.3%) and 3-chloro-1-cyclobutyl-1H-pyrazole-4-carboxylic acid ethyl ester (eluted later, 147 mg, 2.5%). LRMS m/z calcd for C10H13ClN2O2 (M+H) 229.1, found 229.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07728029B2 |
|---|
| Source dataset | uspto-grants-2010_06 |
|---|
| ORD ID | ord-95dec1a9f5d9419baa2798650187c29f |
|---|
| Source note | uspto-grants-2010_06 |
|---|