HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylmorpholine → HCID 18517998, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Reactant | HCID 18517990 | HCID 18517990 | — |
| Reactant | HCID 18518092 | HCID 18518092 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18517998 | HCID 18517998 | — |
Reaction Steps
360 mg of methyl 3-(2-aminoacetylamino)-3-(2-nitrophenyl)propionate hydrochloride are dissolved in 35 ml of DMF, and 190 mg of 4-(4-methylpyridin-2-ylamino)butyric acid are added. After cooling the reaction mixture to 0°, 450 mg of TBTU and 63 mg of HOBt are added. It is neutralized with 0.15 ml of N-methylmorpholine and stirred at room temperature overnight. The solvent is distilled off, and the residue is mixed with 30 ml of ethyl acetate and washed with half-concentrated bicarbonate solution and saturated brine and worked up further as usual. Methyl 3-{2-[4-(4-methylpyridin-2-ylamino)butyrylamino]acetylamino}-3-(2-nitrophenyl)propionate is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06576637B1 |
| Source dataset | uspto-grants-2003_06 |
| ORD ID | ord-54e34fbedc3743798bacc893117acbd7 |
| Source note | uspto-grants-2003_06 |