HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411266Generated: October 27, 2026
4-Methylmorpholine → N-(Toluene-4-sulfonyl)-L-alanyl-L-phenylalanine Benzyl Ester
https://huagongshe.com/reaction/411266
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate | HCID 151348 | — |
| Reactant | Benzyl 3-phenyl-L-alaninate | HCID 736312 | — |
| Reactant | N-Tosyl-L-alanine | HCID 737622 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(Toluene-4-sulfonyl)-L-alanyl-L-phenylalanine Benzyl Ester | HCID 53937992 | 40.3% |
Reaction Steps
To N-(toluene-4-sulfonyl)-L-alanine (2.0 mmoles) in DMF (10 mL) was added BOP (2.1 mmoles) and N-methylmorpholine (4.0 mmoles) and the reaction stirred at room temperature for 45 minutes. L-Phenylalanine benzyl ester (2.0 mmoles) was added and the reaction stirred for 16 hours at room temperature. The reaction mixture was extracted with water (100 mL) and diethyl ether (3×50 mL) The combined organic layers were successively washed with 0.2 N HCl (2×50 mL), sat. NaHCO3 (50 mL), and sat. NaCl (50 mL). The organic layer was dried over MgSO4, filtered, and concentrated to yield a colorless oil (387 mg, 40%). The crude product was purified by silica gel chromatography (50% EtOAc /Hexane, Rf=0.61). The title compound was crystalized from CHCl3/Hexane to yield a white solid, mp=109-110° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06559127B1 |
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| Source dataset | uspto-grants-2003_05 |
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| ORD ID | ord-ad725e2be6674f7db449e0af3efe9b03 |
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| Source note | uspto-grants-2003_05 |
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