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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644361Generated: October 29, 2026

Hydrochloric Acid → [1'-((R)-3-(3,4-diethyl-phenyl)-2-{[4-(2-oxo-1,2,4,5-tetrahydro-1,3-benzodiazepin-3-yl)-piperidine-1-carbonyl]-amino}-propionyl)-[4,4']bipiperidinyl-1-yl]-acetic Acid

https://huagongshe.com/reaction/644361

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactantethyl [1'-((R)-3-(3,4-diethyl-phenyl)-2-{[4-(2-oxo-1,2,4,5-tetrahydro-1,3-benzodiazepin-3-yl)-piperidine-1-carbonyl]-amino}-propionyl)-[4,4']bipiperidinyl-1-yl]-acetateHCID 10485084—
SolventTetrahydrofuranHCID 8028—
Product[1'-((R)-3-(3,4-diethyl-phenyl)-2-{[4-(2-oxo-1,2,4,5-tetrahydro-1,3-benzodiazepin-3-yl)-piperidine-1-carbonyl]-amino}-propionyl)-[4,4']bipiperidinyl-1-yl]-acetic AcidHCID 10078440—

Reaction Steps

A mixture of 150 mg (0.21 mmol) ethyl [1′-((R)-3-(3,4-diethyl-phenyl)-2-{[4-(2-oxo-1,2,4,5-tetrahydro-1,3-benzodiazepin-3-yl)-piperidine-1-carbonyl]-amino}-propionyl)-[4,4′]bipiperidinyl-1-yl]-acetate, 20 mL THF and 2.5 mL 0.1 M NaOH was stirred for 12 h at RT. The organic solvent was eliminated under reduced pressure and the pH of the reaction mixture was adjusted to exactly 7.0 by the addition of 0.1 M HCl. The precipitate was suction filtered, washed with a little water and dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700589B2
Source datasetuspto-grants-2010_04
ORD IDord-e3e6d3639b8848e49a37a44d6e2e37bb
Source noteuspto-grants-2010_04