Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzenepropanoyl chloride | HCID 64801 | — |
| Reactant | HCID 54205135 | HCID 54205135 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 54205135 | HCID 54205135 | — |
| Product | HCID 86634869 | HCID 86634869 | — |
Reaction Steps
Farnesyl-L-Cysteine methyl ester (FCM) was synthesized as described in Ma et al., Methods Enzymol. 250, 226-34 (1995). The FCM (1 g) was dissolved in approximately 100 ml of acetone followed by the addition of triethylamine (TEA, 1 ml) and 1 g of hydrocinnamoyl chloride. This was stirred for 2 h at room temperature. The solvent was removed under reduced pressure, the residue dissolved in 150 ml of ethylacetate and washed three times with water. The ethylacetate layer was dried with anhydrous sodium sulfate, filtered and the ethylacetate removed under reduced pressure. The residue was purified by silica gel chromatography to obtain hydrocinnamoyl-farnesyl-L-Cysteine methyl ester (HCFCM). The purified HCFCM was then analyzed by Electron Spray Ionization Mass Spectrometry (ESI-MS).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07897604B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-e55cd67340af44ccab044c7506a21cfa |
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| Source note | uspto-grants-2011_03 |
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