HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methylimidazole → Argininamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methylimidazole | HCID 1390 | — |
| Reactant | 3-Nitro-1-(2,4,6-trimethylbenzene-1-sulfonyl)-1H-1,2,4-triazole | HCID 716901 | — |
| Reactant | HCID 178454584 | HCID 178454584 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Argininamide | HCID 178512843 | — |
Reaction Steps
Fmoc-Arg(OtBu)-OH, 1-mesitylenesulfonyl-3-nitro-1,2,4-triazole (MSNT) and N-methylimidazole were dissolved in CH2Cl2, and the solution was stirred for 5 minutes and thereafter placed into the solid-phase synthesis column containing the resin, followed by stirring at room temperature for 3 hours. The resin was thereafter washed with methylene chloride, isopropanol and DMF and dried. The unreacted hydroxyl group on the solid phase was thereafter acetylated using a 20% DMF solution of acetic anhydride for 20 minutes for capping. The resin was washed with DMF and stirred along with a 20% piperidine/DMF solution for 20 minutes to remove the protective Fmoc group, whereby resin-Arg-NH2 was obtained. The product was washed with DMF and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07851618B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-f0fbf37c87a6435ca37e8daf56d98dcd |
| Source note | uspto-grants-2010_12 |