HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1493568Generated: October 30, 2026
4-Methylmorpholine → HCID 178479344, compound
https://huagongshe.com/reaction/1493568
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | L-Ornithine, N2-[(1,1-dimethylethoxy)carbonyl]-N5-[imino(nitroamino)methyl]- | HCID 75141 | — |
| Reactant | Ethanol hydrochloride | HCID 21887872 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178479344 | HCID 178479344 | — |
Reaction Steps
Boc Arg(NO2)OH (5.0 g, 15.6 mmol) was dissolved in 60 ml of tetrahydrofuran (THF) and was allowed to react with isobutyl chloroformate (2.06 ml, 15.6 mmol) in the presence of N-methylmorpholine (1.72 ml, 15.6 mmol) for 10 min at -20° C. The mixed anhydride preparation was filtered, and the filtrate was added to 120 ml of ethereal diazomethane. After stirring the reaction solution for 30 min at 0° C., 80 ml of ether was added. The product crystallized from the reaction solution in the cold. The Boc-Arg(HO2)CHNH2 product was dissolved in a minimum volume of THF and was allowed to react with ethanol HCl (20 mmol) at room temperature until nitrogen evolution ceased.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05023236 |
|---|
| Source dataset | uspto-grants-1991_06 |
|---|
| ORD ID | ord-f5ac0f6aeb734f449c225bf22b32321d |
|---|
| Source note | uspto-grants-1991_06 |
|---|