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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 84211Generated: October 31, 2026

Hydrochloric Acid → 5-[(R)-1-Biphenyl-4-ylmethyl-2-(1-butoxycarbonyl-cyclopropyl)-ethylcarbamoyl]-1H-pyrazole-3-carboxylic acid

https://huagongshe.com/reaction/84211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantPyrazole-3,5-dicarboxylic acidHCID 76559—
Reactant1-((R)-3-Biphenyl-4-yl-2-t-butoxycarbonylaminopropyl)cyclopropanecarboxylic acid t-butyl esterHCID 68180869—
Solvent1-ButanolHCID 263—
SolventDimethylformamideHCID 6228—
Solvent1,4-DioxaneHCID 31275—
Product5-[(R)-1-Biphenyl-4-ylmethyl-2-(1-butoxycarbonyl-cyclopropyl)-ethylcarbamoyl]-1H-pyrazole-3-carboxylic acidHCID 17845074195%

Reaction Conditions

Temperature65 °C

Reaction Steps

1-((R)-3-Biphenyl-4-yl-2-t -butoxycarbonylaminopropyl)cyclopropanecarboxylic acid t-butyl ester (1.0 g, 2.2 mmol, 1.0 eq.), 1-butanol (5 mL) and 4 M of HCl in 1,4-dioxane (2 mL) were combined and stirred at 65° C. overnight. To this was added a mixture of 3,5-pyrazoledicarboxylic acid (34.6 mg, 221 mmol, 1.0 eq.), EDCI (39.2 mL, 221 mmol, 1.0 eq.) and HOBt (29.9 mg, 221 mmol, 1.0 eq.) that had been combined in DMF (0.2 mL) and stirred for 5 minutes at room temperature. The resulting mixture was stirred for 30 minutes. The reaction was then quenched with ACOH and the product was purified by preparative HPLC and lyophilized to yield the title compound (29 mg, 95% purity). MS m/z [M+H]+ calc'd for C28H31N3O5, 490.23; Found 490.6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846913B2
Source datasetuspto-grants-2014_09
ORD IDord-4ea5be69091d4e85abc951f141d1a129
Source noteuspto-grants-2014_09