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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2230319Generated: November 1, 2026

4-Nitrobenzenesulfonyl chloride → 3-(4-Benzyloxy-phenyl)-2-[4-methyl-2-(4-nitro-benzenesulfonylamino)-pentanoylamino]-propionic acid tert-butyl ester

https://huagongshe.com/reaction/2230319

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrobenzenesulfonyl chlorideHCID 7404—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-(2-Amino-4-methyl-pentanoylamino)-3-(4-benzyloxy-phenyl)-propionic acid tert-butyl esterHCID 54081729—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventBenzeneHCID 241—
Solventtert-Butyl methyl etherHCID 15413—
Product3-(4-Benzyloxy-phenyl)-2-[4-methyl-2-(4-nitro-benzenesulfonylamino)-pentanoylamino]-propionic acid tert-butyl esterHCID 7005913495%

Reaction Steps

A solution of the product from Example AI ([S-(R*,R*)]-2-(2-amino-4-methyl-pentanoylamino)-3-(4-benzyloxy-phenyl)-propionic acid tert-butyl ester) (308 mg, 0.70 mmol), 4-nitrobenzenesulfonyl chloride (190 mg, 0.77 mmol), N,N-diisopropylethyl-amine (181 mg, 1.4 mmol) and DMAP (20 mg), in benzene (5 mL) was heated under reflux for 3 hours, then concentrated in vacuo and the residue dissolved in ethyl acetate, and washed with saturated NaHCO3 solution, water, and brine, dried over anhydrous sodium sulfate, and concentrated in vacuo. The tan solid thus obtained was triurated in warm tert-butylmethyl ether, and filtered to give 419 mg (95%) of the title compound as a white solid, mp=121-123° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06423689B1
Source datasetuspto-grants-2002_07
ORD IDord-8b8c24e72b38407abd457f23b161690b
Source noteuspto-grants-2002_07