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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803777Generated: November 1, 2026

Dichloromethane → HCID 178439315, compound

https://huagongshe.com/reaction/1803777

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant2,6-LutidineHCID 7937—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantHOAtHCID 181649—
Reactant(3R)-3-Amino-4-phenylbutanoic acid--hydrogen chloride (1/1)HCID 24820568—
ReactantHCID 178439323HCID 178439323—
ProductHCID 178439315HCID 17843931592%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 5-propyl-1-[2′-(1H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-1H-pyrazole-3-carboxylic acid (200 mg, 510 μmol), HOAt (77.1 mg, 566.4 μmol), EDCI (108.6 mg, 566.4 μmol), and 2,6-lutidine (357.8 μL, 3.1 mmol) in DCM (6.1 mL, 94.7 mmol) was stirred to pre-activate the acid. After 30 minutes, the mixture was cooled at 0° C. and (R)-3-amino-4-phenylbutyric acid hydrochloride (122.2 mg, 566.4 μmol) was added. The resulting solution was slowly warmed to room temperature and stirred overnight. The mixture was then concentrated, re-dissolved in water/MeCN/TFA and purified using reverse phase liquid chromatography to yield the title compound (59 mg; 92% purity). MS m/z: [M+H]+ calcd for C31H31N7O3, 550.25; found 550.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08350027B2
Source datasetuspto-grants-2013_01
ORD IDord-1368bae789d44b61a00acde52d1fb102
Source noteuspto-grants-2013_01