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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2366331Generated: October 29, 2026

Hydrochloric Acid → 5-({3-[4-(Biphenyl-2-ylcarbamoyloxy)piperidin-1-yl]-propionyl}methylamino)pentanoic acid

https://huagongshe.com/reaction/2366331

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantLithium HydroxideHCID 3939—
Reactanttert-ButanolHCID 6386—
Reactant5-({3-[4-(Biphenyl-2-ylcarbamoyloxy)piperidin-1-yl]propionyl}-methylamino)pentanoic acid methyl esterHCID 66770099—
SolventWaterHCID 962—
Product5-({3-[4-(Biphenyl-2-ylcarbamoyloxy)piperidin-1-yl]-propionyl}methylamino)pentanoic acidHCID 66781801—

Reaction Steps

To a mixture of 5-({3-[4-(biphenyl-2-ylcarbamoyloxy)piperidin-1-yl]propionyl}-methylamino)pentanoic acid methyl ester (10.21 g, 20.60 mmol), tert-butyl alcohol (20 mL) and water (20 mL) was added a 1:1 mixture of LiOH:water (1.97 g, 41.2 mmol). The resulting mixture was stirred at room temperature for 4 h and then the pH of the mixture was adjusted to about pH 2 using aqueous hydrochloric acid (1 N). The aqueous layer was extracted with DCM (2ט80 mL) and the organic layers were combined, dried over sodium sulfate, filtered, and concentrated under reduced pressure to give the title compound (12.23 g, quantitative) as an off-white foamy solid (containing residual tert-butyl alcohol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697724B2
Source datasetuspto-grants-2014_04
ORD IDord-851372b076a3423198a1b7f2a2abea4e
Source noteuspto-grants-2014_04