HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylmorpholine → N-Benzenesulfonyl-(L)-prolyl-2-amino-2-norbornanecarboxylic acid, methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | (2S)-1-(Benzenesulfonyl)pyrrolidine-2-carboxylic acid | HCID 720844 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 86759759 | HCID 86759759 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-Benzenesulfonyl-(L)-prolyl-2-amino-2-norbornanecarboxylic acid, methyl ester | HCID 86759758 | 59% |
Reaction Steps
To a solution of 2-amino-2-norbornanecarboxylate, methyl ester hydrochloride (400 mg, 2.0 mmol), N-benzenesulfonyl-(L)-proline (510 mg, 2.0 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (306 mg, 2.0 mmol), 1-hydroxbenzotriazole (202 mg, 2.0 mmol) in 4 mL of tetrahydrofuran at 0° C. was added N-methyl morpholine (0.22 mL, 2.0 mmol). After 15 min at 0° C., the reaction mixture was stirred at room temperature for 16 h, and was concentrated in vacuo. The residue was purified by flash column chromatography on silica gel eluted with 10:1 methylene chloride/ethyl acetate to give the title compound (478 mg, 59%) as a mixture of diastereomers.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06903075B1 |
| Source dataset | uspto-grants-2005_06 |
| ORD ID | ord-6921d2ce58384a119f112e8892218a20 |
| Source note | uspto-grants-2005_06 |