HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378452Generated: October 31, 2026
Dicyclohexylcarbodiimide → HCID 10552575, compound
https://huagongshe.com/reaction/1378452
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | HOAt | HCID 181649 | — |
| Reactant | 1-Sulfanylcyclopentane-1-carboxylic acid | HCID 15817584 | — |
| Reactant | HCID 86749398 | HCID 86749398 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 10552575 | HCID 10552575 | — |
Reaction Steps
To a stirred solution of 1-mercapto-1-cyclopentanecarboxylic acid (1.74 g, 4.54 mmol) in dichloromethane (50 mL) and triethylamine (0.63 mL) is added [(1-amino-(1-cyclopentyl)carbonyl]-L-tyrosine butyl ester hydrochloride (0.66 g). To this solution is added 1-hydroxy-7-azabenzotriazole (0.68 g, 4.55 mmol) and 1,3-dicyclohexylcarbodiimide (1.03 g, 4.99 mmol). The mixture is stirred for 14 hours and then the solid precipitate is removed by filtration. The organic phase is washed with a saturated solution of sodium bicarbonate (10 mL), brine (10 mL), dried over magnesium sulfate and the solvent is removed to give a clear oil. The oil is purified by flash chromatography (SiO2, hexane/ethyl acetate, 6:4) to give a clear foam. The foam is crystallized from ethyl ether to yield N-[[1-[[(1-mercapto-1-cyclopentyl)carbonyl]amino]-1-cyclopentyl]carbonyl]-L-tyrosine butyl ester, m.p. 106°-107° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05668158 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-e5e927817a2744be940cd68c5d7fc6c7 |
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| Source note | uspto-grants-1997_09 |
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