Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Amantadine | HCID 2130 | — |
| Reactant | N-Ethyl-N-[(heptadecafluorooctyl)sulphonyl]glycine | HCID 18134 | — |
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22639319 | HCID 22639319 | — |
Reaction Steps
30.95 g (150 mmol) of N,N-dicyclohexylcarbodiimide is added at 0° C. to 15.12 g (100 mmol) of 1-aminoadamantane, 58.52 g (100 mmol) of N-(ethyl)N-(perfluorooctylsulfonyl)-aminoacetic acid and 11.51 g (100 mmol) of N-hydroxysuccinimide, dissolved in 300 ml of tetrahydrofuran. It is stirred for 2 hours at 0° C., then for 6 hours at room temperature. Precipitated urea is filtered out, the filtrate is evaporated to the dry state, and the residue is chromatographed on silica gel (mobile solvent: dichloromethane/acetone=30:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06818203B2 |
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| Source dataset | uspto-grants-2004_11 |
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| ORD ID | ord-527e05b2b6c84f8cbf2b5a7b33a08af7 |
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| Source note | uspto-grants-2004_11 |
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