Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396984Generated: November 2, 2026

Hydrochloric Acid → (3R)-3-(cyclopentylmethyl)-4-[5-(4-morpholinylcarbonyl)-4,5-dihydro-1H-pyrazol-1-yl]-4-oxobutanoic acid

https://huagongshe.com/reaction/1396984

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,1-dimethylethyl (3R)-3-(cyclopentylmethyl)-4-[5-(4-morpholinylcarbonyl)-4,5-dihydro-1H-pyrazol-1-yl]-4-oxobutanoateHCID 68287991—
Solvent1,4-DioxaneHCID 31275—
Product(3R)-3-(cyclopentylmethyl)-4-[5-(4-morpholinylcarbonyl)-4,5-dihydro-1H-pyrazol-1-yl]-4-oxobutanoic acidHCID 68288029100%

Reaction Steps

To 1,1-dimethylethyl (3R)-3-(cyclopentylmethyl)-4-[5-(4-morpholinylcarbonyl)-4,5-dihydro-1H-pyrazol-1-yl]-4-oxobutanoate (244 mg, 0.58 mmol) in 1,4-dioxane (5.0 mL) was added 4.0 M hydrochloric acid in 1,4-dioxane (7.25 mL, 29.0 mmol) at room temperature. The resulting reaction mixture was stirred for 4 hours. The solvent was then removed by reduced pressure to afford the crude product (3R)-3-(cyclopentylmethyl)-4-[5-(4-morpholinylcarbonyl)-4,5-dihydro-1H-pyrazol-1-yl]-4-oxobutanoic acid (212 mg, 0.58 mmol, 100% yield), which was used directly in the next step. MS: 366 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901119B2
Source datasetuspto-grants-2014_12
ORD IDord-f4fd4328f1fd45cc89d681e27415b3c9
Source noteuspto-grants-2014_12