HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylmorpholine → Boc-Pro-Gly-NH2
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1,2-Pyrrolidinedicarboxylic acid, 1-(1,1-dimethylethyl) ester, (2S)- | HCID 85083 | — |
| Reactant | Glycinamide hydrochloride | HCID 2723639 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Boc-Pro-Gly-NH2 | HCID 7256544 | — |
Reaction Steps
0.56 mg (5 mmol) of H-Gly-NH2.HCl are dissolved in 20 ml MeOH and 270 mg (5 mmol) NaOMe added. Stirring takes place for 10 min and the solvent is removed under vacuum. To the residue are added 15 ml DMF, 1.07 g (5 mmol) Boc-Pro-OH, 1.2 g (6.0 mmol) EDCI, 0.9 g (6 mmol) HOBT and 0.825 ml (7.5 mmol) NMM and stirring takes place for 16 hours. To the reaction mixture are added 10 g of mixed-bed ion exchanger (Merck ion exchanger V), stirring takes place for 0.5 hours, followed by filtering and washing with 10 ml MeOH. The filtrate is concentrated under vacuum, the resulting oil absorbed in 150 ml ethyl acetate and the organic phase washed three times with 10 ml 0.5N HCl, 10% NaHCO3 solution and H2O respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05556836 |
| Source dataset | uspto-grants-1996_09 |
| ORD ID | ord-c1fdc066edbf4779a8cb11ae4b5999b7 |
| Source note | uspto-grants-1996_09 |