HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-BOC-ethylenediamine → n-Boc-2-aminoethylguanidine hydroiodide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-BOC-ethylenediamine | HCID 187201 | — |
| Reactant | S-methylthiouronium iodide | HCID 197812 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | n-Boc-2-aminoethylguanidine hydroiodide | HCID 23513565 | 72.8% |
Reaction Steps
A solution of commercial N-BOC-ethylendiamine (1 g) in dry ethanol (100 ml) and 2-methyl-2-thiopseudourea hydroiodide (1.5 g) was refluxed for 8 hours. The solvent was removed at reduced pressure and the crude residue purified by flash chromatography (methylene chloride/methanol:9/1) to yield 1.5 g of N-BOC-2-aminoethylguanidine hydroiodide as a yellow oil which was dissolved in methanolic hydrochloric acid solution 5N (20 ml) and stirred at room temperature for 3 hours. The white precipitate was collected and washed with dry ethanol, affording 700 mg of the intermediate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06458768B1 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-46b66cff4c0c4a838d8ca41fcd55ffaa |
| Source note | uspto-grants-2002_10 |