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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786802Generated: October 31, 2026

Hydrochloric Acid → Biphenyl-2-ylcarbamic Acid

https://huagongshe.com/reaction/1786802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiisopropylethylamineHCID 81531—
ReactantPyBOPHCID 2724699—
Reactant3-[4-(Biphenyl-2-ylcarbamoyloxy)piperidin-1-yl]propionic AcidHCID 21880607—
Reactant5-[(R)-2-[(5-Aminopentyl)benzylamino]-1-(tert-butyldimethylsilanyloxy) ethyl]-8-benzyloxy-1H-quinolin-2-oneHCID 66968054—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductBiphenyl-2-ylcarbamic AcidHCID 607059408%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of the product of step (e) (3.68 g, 10 mmol) and N,N-dimethylformamide (50 mL) was heated at 60° C. until the solid completely dissolved and then cooled to room temperature. The product of step (d) (6 g, 10 mmol) and diisopropylethylamine (3.5 mL) was added and the reaction mixture was cooled to 0° C. PyBOP (6.25 g, 12 mmol) was added in one portion and the reaction mixture was stirred at 0° C. to room temperature for 2 hours. The reaction mixture was then poured into cold water (500 mL) with stirring and the pH of the resulting mixture was adjusted to about 2 using aqueous 1 M hydrochloric acid. This mixture was stirred for 15 min and then filtered to collect the solid, which was washed with water (100 mL) and dried to afford the title compound (8.7 g, HPLC purity >95%) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07507751B2
Source datasetuspto-grants-2009_03
ORD IDord-9c76de6b15aa48ca98ce587051bf7c2c
Source noteuspto-grants-2009_03