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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2281163Generated: November 3, 2026

Hydrochloric Acid → HCID 71239397, compound

https://huagongshe.com/reaction/2281163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 71239892HCID 71239892—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 71239397HCID 7123939774.4%

Reaction Steps

(+/−)-3-{4-[(3,3-Dimethyl-cyclobutyl)-(6-fluoro-3-methyl-quinolin-2-ylamino)-methyl]-benzoylamino}-propionic acid ethyl ester (14.3 mg, 0.029 mmol), made in a similar manner as Intermediate 27 from Intermediate 29, was dissolved in tetrahydrofuran (1.5 mL) and methanol (0.5 mL), and 1.0 M sodium hydroxide (1 mL) was added. This was stirred as a solution at room temperature for 20 min before 1 N HCl was added to bring to pH 5. This was extracted twice with ethyl acetate and the combined organics dried over MgSO4, and concentrated in vacuo. Purification by reversed-phase HPLC gave (+/−)-3-{4-[(3,3-dimethyl-cyclobutyl)-(6-fluoro-3-methyl-quinolin-2-ylamino)-methyl]-benzoylamino}-propionic acid (10 mg). Analytical LCMS: retention time 2.3998 minutes (Waters Atlantic dC18 4.6×50 mm, 5 μm column; 5% acetonitrile/water (0.05% trifluoroacetic acid modifier) linear gradient to 95% acetonitrile/water over 4.0 minutes, hold at 95% acetonitrile/water for 1.0 minute; flow rate 2.0 mL/minute); MS (M+1): 464.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139538B2
Source datasetuspto-grants-2015_09
ORD IDord-bef2aca4d59b4b93a09951c471a41d9b
Source noteuspto-grants-2015_09