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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700655Generated: October 31, 2026

L-Pyroglutamic Acid → HCID 178428125, compound

https://huagongshe.com/reaction/1700655

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-Pyroglutamic AcidHCID 7405—
ReactantHCID 178428123HCID 178428123—
SolventEthanolHCID 702—
ProductHCID 178428125HCID 17842812571.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of (±)-7-(2,5-dichlorothiophen-3-yl)-5-guanidinoimino-4-methyl-5,6,7,8-tetrahydroquinoline (17.4 g) in ethanol (200 ml) was added a solution of L-pyroglutamic acid (4.0 g) in ethanol (20 ml), at 80° C., and the mixture was gradually cooled to the room temperature and stirred at room temperature for 6 hours. The crystals were filtered and washed with ethanol to give (+)-7-(2,5-dichlorothiophen-3-yl)-5-guanidinoimino-4-methyl-5,6,7,8-tetrahydroquinoline L-pyroglutamate (11.0 g). Said crystals were suspended in methanol (200 ml), and to the mixture was added a solution of 28% sodium methoxide in methanol (4.2 ml). Under reduced pressure, the solvent was evaporated to give crystals, which were washed with water, dried and recrystallized from ethanol. To the crystals was added ethanol (30 ml), and then methanesulfonic acid (3.4 g). The mixture was heated to give a homogenous solution and cooled, and precipitated crystals were filtered to give (+)-7-(2,5-dichlorothiophen-3-yl)-5-guanidinoimino-4-methyl-5,6,7,8-tetrahydroquinoline methanesulfonate (Compound 111) (8.5 g, 99.9% ee).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06350749B1
Source datasetuspto-grants-2002_02
ORD IDord-686309dddf80420c915638554d4ca74a
Source noteuspto-grants-2002_02