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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49200Generated: October 29, 2026

L-Pyroglutamic Acid → HCID 178428134, compound

https://huagongshe.com/reaction/49200

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-Pyroglutamic AcidHCID 7405—
ReactantHCID 178428132HCID 178428132—
SolventEthanolHCID 702—
ProductHCID 178428134HCID 17842813442%

Reaction Steps

A solution of (±)-7-(2-chloro-5-fluorophenyl)-5-guanidinoimino-4-methyl-5,6,7,8-tetrahydroquinoline (7.1 g) in ethanol (85 ml) was combined with L-pyroglutamic acid (2.72 g) and heated to form a uniform solution. The mixture was allowed to stand to cool gradually, and stirred at room temperature for 14 hours. The crystal precipitated was recovered by a filtration and washed with ethanol to obtain (+)-7-(2-chloro-5-fluorophenyl)-5-guanidinoimino-4-methyl-5,6,7,8-tetrahydroquinoline L-pyroglutamate (4.1 g). This crystal was suspended in methanol (50 ml) and combined with a 28% solution of sodium methoxide in methanol (1.7 g) and then the solvent was distilled off under reduced pressure. The resultant crystal was washed with water and dried to obtain a crystal (3.1 g). This was dissolved in ethanol (20 ml) and combined with methanesulfonic acid (1.8 g). The solvent was distilled off under reduced pressure, and the resultant crystal was recrystallized from ethanol to obtain (+)-7-(2-chloro-5-fluorophenyl)-5-guanidinoimino-4-methyl-5,6,7,8-tetrahydroquinoline methanesulfonate (Compound H)(3.6 g, 99.3% ee).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706732B1
Source datasetuspto-grants-2004_03
ORD IDord-f22373ef009c4ad394520835f6116971
Source noteuspto-grants-2004_03