HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2402923Generated: October 31, 2026
3-Amino-5-chloro-2-hydroxybenzenesulfonic acid → N5-(2-hydroxy-3-sulfophenyl)-L-glutamine
https://huagongshe.com/reaction/2402923
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Amino-5-chloro-2-hydroxybenzenesulfonic acid | HCID 6927 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | (4S)-5-(Benzyloxy)-4-(((benzyloxy)carbonyl)amino)-5-oxopentanoic acid | HCID 6994031 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N5-(2-hydroxy-3-sulfophenyl)-L-glutamine | HCID 123937419 | 40% |
Reaction Steps
Z-Glu-OBn (371 mg, 1 mmol) was dissolved in methylene chloride (1 mL), and CDI (180 mg, 1.1 mmol) was added thereto and stirred at room temperature for 30 minutes. Then, 2-amino-4-chlorophenol-6-sulfonic acid (223 mg, 1 mmol) and THF (1 mL) were added thereto and stirred overnight at room temperature. After removing a solvent, purification was conducted in accordance with the purification process A. The obtained intermediate was dissolved in a mixed solvent of methanol and water. Pd/C in catalyst quantity was added thereto and stirred under hydrogen atmosphere overnight at room temperature. After filtering out the catalyst and removing a solvent, purification was conducted in accordance with the purification process A to obtain a title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08796485B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-20673dadf79144aeb0ceb30a1c0fb88c |
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| Source note | uspto-grants-2014_08 |
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