HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1356870Generated: October 27, 2026
4-Toluenesulfonyl chloride → N-(Toluene-4-sulfonyl)-L-prolyl-L-phenylalanine N-(Toluene4-sulfonyl)amide
https://huagongshe.com/reaction/1356870
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-(toluene-4-sulfonyl)-L-prolyl-L-phenylalanine amide | HCID 54382446 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(Toluene-4-sulfonyl)-L-prolyl-L-phenylalanine N-(Toluene4-sulfonyl)amide | HCID 54500258 | — |
Reaction Steps
N-(Toluene-4-sulfonyl)-L-proline was reacted with L-phenylalanine amide using the procedure described in Method 12 to yield N-(toluene-4-sulfonyl)-L-prolyl-L-phenylalanine amide. To a solution of NaH (60% mineral oil—prewashed with THF) in THF at 0° C. was added N-(toluene-4-sulfonyl)-L-prolyl-L-phenylalanine amide and the reaction was stirred at 0° C. for 45 minutes. Toluene-4-sulfonyl chloride was added and the reaction was stirred for 16 hours at room temperature. The reaction mixture was extracted with EtOAc (3×50 mL) and 0.2 N HCl (50 mL), and the combined organic layers were washed successively with sat. NaHCO (50 mL), and sat. NaCl (2×50 mL), dried over MgSO4, filtered, and concentrated to yield the title compound as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06586602B2 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-78baf102872f4af2b704edb7f95a2487 |
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| Source note | uspto-grants-2003_07 |
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