HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732518Generated: November 1, 2026
Ninhydrin → Benzyloxycarbonyl-L-valyl-L-leucyl-L-threonine methyl ester
https://huagongshe.com/reaction/1732518
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ninhydrin | HCID 10236 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Z-Val-ONp | HCID 112124 | — |
| Reactant | Benzyloxycarbonyl-L-leucyl-L-threonine methyl ester | HCID 54439782 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Benzyloxycarbonyl-L-valyl-L-leucyl-L-threonine methyl ester | HCID 53923485 | — |
Reaction Steps
Benzyloxycarbonyl-L-leucyl-L-threonine methyl ester (I, 3.8 g, 10 mmole) was dissolved in a mixture of 95% EtOH (50 ml) and 1 N HCl (10 ml) and hydrogenated in the presence of a 10% Pd on charcoal catalyst (0.8 g). After removal of the catalyst and the solvent the residue was dissolved in DMF (35 ml), treated with DIEA (1.6 ml, 10 mmole), benzyloxycarbonyl-L-valine p-nitrophenyl ester (4.3 g, 12 mmole) and HOBt (1.5 g, 10 mmole). After a negative spot test with ninhydrin indicated the completion of the reaction, the solvent was removed in vacuo and the residue triturated with CHCl3 (40 ml). The resulting solid was washed with CHCl3 (20 ml) and dried: 4.5 g (94%, mp 217°-8° C.,) unchanged after extraction with solvents, [α]D24 -11.7° (c 1.5, DMF); RfC 0.75; Thr 1.08; Val 0.98; Leu 1.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04237046 |
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| Source dataset | uspto-grants-1980_12 |
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| ORD ID | ord-065fcdcd96ec4e4f8d0f437e82a1a642 |
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| Source note | uspto-grants-1980_12 |
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