HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700655Generated: October 31, 2026
L-Pyroglutamic Acid → HCID 178428125, compound
https://huagongshe.com/reaction/1700655
Participants
| Role | Name | HCID | Charge |
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| Reactant | L-Pyroglutamic Acid | HCID 7405 | — |
| Reactant | HCID 178428123 | HCID 178428123 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178428125 | HCID 178428125 | 71.4% |
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
| 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-686309dddf80420c915638554d4ca74a |
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| Source note | uspto-grants-2002_02 |
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