HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1596739Generated: October 29, 2026
Dicyclohexylcarbodiimide → HCID 131632219, compound
https://huagongshe.com/reaction/1596739
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Reactant | Benzyl glycinate | HCID 409140 | — |
| Reactant | N-(tert-Butoxycarbonyl)glycyl-L-phenylalanyl-L-leucine | HCID 13943016 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Solvent | p-Toluenesulfonate | HCID 85570 | — |
| Product | HCID 131632219 | HCID 131632219 | 62.3% |
Reaction Steps
The Boc-Gly-Phe-Leu-OH obtained in Example 18 (2.4 g) and N-hydroxysuccinimide (656 mg) were dissolved in N,N-dimethylformamide (50 ml), cooled to 4° C., and then added with N,N′-dicyclohexylcarbodiimide (1.17 g), and stirred for 2 hours. To this solution, a N,N-dimethylformamide solution (40 ml) in which tosylate of H-Gly-OBzl (1.9 g) and triethylamine (0.79 ml) had been dissolved was added, and the mixture was allowed to react with stirring at room temperature for 16 hours. This reaction mixture was evaporated to dryness under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: dichloromethane:methanol=50:1 solution) to give the title compound (2.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06291671B1 |
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| Source dataset | uspto-grants-2001_09 |
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| ORD ID | ord-0cf8212055c34a51813f2315b3c87848 |
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| Source note | uspto-grants-2001_09 |
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