HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1698764Generated: October 30, 2026
HCID 70183495, compound → HCID 70182935, compound
https://huagongshe.com/reaction/1698764
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 70183495 | HCID 70183495 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 70182935 | HCID 70182935 | 76% |
Reaction Steps
(±)-2-tert-Butoxycarbonylamino-3-(2-nitrophenyl)-amin opropionic acid (325 mg) was dissolved in methanol (50 mL), followed by the addition of 10% palladium carbon (50 mg). The resulting mixture was stirred at room temperature for 1 hour under a hydrogen atmosphere. The reaction mixture was filtered and the filtrate was concentrated under reduced pressure, whereby (±)-2-tert-butoxycarbonylamino-3-(2-aminophenyl)-aminopropi onic acid was obtained. It was suspended in toluene (30 mL) The suspension was refluxed for 3 hours while removing water by a Dean-Stark extractor. The resultant mixture was concentrated under reduced pressure. After the residue was purified by silica gel colomn chromatography (chloroform:methanol=20:1), diisopropyl ether was added thereto for crystallization. Crystals so precipitated were then collected by filtration, whereby the title compound (210 mg) was obtained. Yield: 76%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06344452B1 |
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| Source dataset | uspto-grants-2002_02 |
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| ORD ID | ord-3cff3304a4d54e3f8b10cfb0aa8b2569 |
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| Source note | uspto-grants-2002_02 |
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