HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375339Generated: October 27, 2026
Dicyclohexylcarbodiimide → N-lysyl-5'-O-palmitoyl-deoxycytidine
https://huagongshe.com/reaction/1375339
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 5'-O-palmitoyldeoxycytidine | HCID 15484389 | — |
| Reactant | Di-tert-butoxycarbonyl-lysine | HCID 22792075 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | N-lysyl-5'-O-palmitoyl-deoxycytidine | HCID 15484390 | — |
Reaction Steps
14 grams of 5′-O-palmitoyl-deoxycytidine is dissolved in 100 ml dimethylacetamide, 1 molar equivalent of di-tert-butoxycarbonyl-lysine is added, and the mixture is cooled in an ice bath. 1.2 molar equivalents (7.4 g) of dicyclohexylcarbodiimide are added and the mixture is stirred at 4° C. for 90 hours. The precipitate (dicyclohexylurea) is removed by filtration. 100 ml of water is added to the filtrate, followed by 1 liter of ethyl acetate. N4-(di-N-tert-butoxycarbonyl-lysyl)-5′-O-palmitoyl-deoxycytidine is separated from unreacted reagents by chromatography over silica gel. The t-butoxycarbonyl protecting groups are removed by the standard methods of treatment with an acid, such as trifluoroacetic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07169765B1 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-2d910789483e4b29bc34e61d8434cae0 |
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| Source note | uspto-grants-2007_01 |
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