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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279715Generated: October 27, 2026

4-Toluenesulfonyl chloride → N-(Toluene-4-sulfonyl)-L-prolyl-L-phenylalanine N-(Toluene4-sulfonyl)amide

https://huagongshe.com/reaction/279715

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantSodium hydrideHCID 24758—
ReactantN-(toluene-4-sulfonyl)-L-prolyl-L-phenylalanine amideHCID 54382446—
SolventTetrahydrofuranHCID 8028—
ProductN-(Toluene-4-sulfonyl)-L-prolyl-L-phenylalanine N-(Toluene4-sulfonyl)amideHCID 54500258—

Reaction Conditions

Temperature0 °C

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. NaHCO3 (50 mL), and sat. NaCl (2×50 mL), dried over MgSO4, filtered, and concentrated to yield the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06362341B1
Source datasetuspto-grants-2002_03
ORD IDord-7a22beb62111452fb8de0b257796189f
Source noteuspto-grants-2002_03