HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700731Generated: November 1, 2026
L-Pyroglutamic Acid → HCID 178428152, compound
https://huagongshe.com/reaction/1700731
Participants
| Role | Name | HCID | Charge |
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| Reactant | L-Pyroglutamic Acid | HCID 7405 | — |
| Reactant | HCID 178428150 | HCID 178428150 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178428152 | HCID 178428152 | 55.6% |
Reaction Steps
To a solution of (±)-7-(3,5-dichlorothiophen-2-yl)-5-guanidinoimino-4-methyl-5,6,7,8-tetrahydroquinoline (1.6 g) in ethanol (10 ml) was added a solution of L-pyroglutamic acid (0.56 g) in ethanol (2 ml) at 80° C., and the mixture was gradually cooled to room temperature and stirred at room temperature for 6 hours. The resulting crystals were filtered and washed with ethanol to give (+)-7-(3,5-dichlorothiophen-2-yl)-5-guanidinoimino-4-methyl-5,6,7,8-tetrahydroquinoline L-pyroglutamate (1.2 g). Said crystals were recrystallized from ethanol and suspended in methanol, and to the suspension was added a solution of 28% sodium methoxide in methanol (0.6 g). Under reduced pressure, the solvent was evaporated. The resulting crystals were washed with water, dried and dissolved in ethanol (10 ml). To the solution was added methanesulfonic acid (0.098 g), and the mixture was concentrated. The resulting crystals were recrystallized from ethanol to give (+)-7-(3,5-dichlorothiophen-2-yl)-5-guanidinoimino-4-methyl-5,6,7,8-tetrahydroquinoline methanesulfonate (Compound 143) (0.1 g,99.6%ee).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06350749B1 |
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| Source dataset | uspto-grants-2002_02 |
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| ORD ID | ord-c44dbe24ec584bd9b6f568bddc2c51c1 |
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| Source note | uspto-grants-2002_02 |
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