HuagongsheHuagongshe Chemistry Print Report · For research reference only
Glycine → HCID 178427602, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Glycine | HCID 750 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | L-Ornithine, N2-[(1,1-dimethylethoxy)carbonyl]-N5-[imino[[(4-methylphenyl)sulfonyl]amino]methyl]- | HCID 83767 | — |
| Reactant | HCID 178418600 | HCID 178418600 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | dichloromethane N,N-dimethylformamide | HCID 22350042 | — |
| Product | HCID 178427602 | HCID 178427602 | — |
Reaction Steps
Condensation with arginine and BOC-deprotection. The Gly-resin is suspended in 200 ml of methylene chloride and treated with a triple-molar quantity respect to the glycine of the second amino acid (first amino acid of the sequence desired), adding a solution of 9.85 g (23 mmol) of BOC-Nω -tosyl-L-arginine in 60 ml of DMF:CH2Cl2 1:1. After 10 minutes under agitation, 4.76 g (23 mmol) of DCCD dissolved in 30 ml of methylene chloride are added and left under agitation at room temperature for 20 hours. The resin is then filtered and washed with CH2Cl2 and with ethanol, then vacuum-dried obtaining 12.3 g of BOC-Nω -tosyl-L-arginine-glycine-resin which, when controlling with ninhydrin, confirms the absence of free amine groups.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04784988 |
| Source dataset | uspto-grants-1988_11 |
| ORD ID | ord-120052bb8202415e8454131e383cb1ed |
| Source note | uspto-grants-1988_11 |