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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298177Generated: October 30, 2026

HCID 53697450, compound → HCID 22246720, compound

https://huagongshe.com/reaction/2298177

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 53697450HCID 53697450—
Solvent1,4-Dioxane hydrochlorideHCID 20443148—
ProductHCID 22246720HCID 2224672013.6%

Reaction Steps

A solution of [3-(2-{[3-(3-chloro-phenyl)-propyl]-methanesulfonyl-amino}-ethyl)-phenyl]-acetic Acid tert-butyl ester (170 mg, 0.36 mmol) in HCl/dioxane (5 mL) was stirred for 48 h at room temperature. The reaction was concentrated and the residue was taken up in dilute aqueous NaOH (10 mL, pH=9.3). The aqueous solution was washed with EtOAc (10 mL) and the layers were separated. The aqueous layer after extraction with EtOAc (10 mL) was acidified with dilute aqueous HCl to a pH of 2.5. After extraction of the acidic aqueous layer with EtOAc (10 mL) the organic solution was dried over MgSO4, filtered, and concentrated to afford the title compound as an oil (20 mg). 1H NMR (400 MHz, CDCl3) δ 6.90-7.50 (m, 8H), 3.00-3.30 (m, 4H), 2.95 (s, 3H), 2.45-2.85 (m, 4H), 1.80 (m, 2H); MS 408 (M−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492412B2
Source datasetuspto-grants-2002_12
ORD IDord-fbec229a70d749bbba7fe8a19e3ef1ed
Source noteuspto-grants-2002_12