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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1865722Generated: October 27, 2026

N,beta,beta-trimethyl-L-phenylalanyl-N1-[(1S,2E)-3-(ethoxysulfonyl)-1-isopropylprop-2-enyl]-N1,3-dimethyl-L-valinamide → N,beta,beta-trimethyl-L-phenylalanyl-N1-[(1S,2E)-1-isopropyl-3-sulfoprop-2-enyl]-N1,3-dimethyl-L-valinamide

https://huagongshe.com/reaction/1865722

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,beta,beta-trimethyl-L-phenylalanyl-N1-[(1S,2E)-3-(ethoxysulfonyl)-1-isopropylprop-2-enyl]-N1,3-dimethyl-L-valinamideHCID 11706341—
CatalystTetrabutylammonium IodideHCID 67553—
SolventAcetoneHCID 180—
ProductN,beta,beta-trimethyl-L-phenylalanyl-N1-[(1S,2E)-1-isopropyl-3-sulfoprop-2-enyl]-N1,3-dimethyl-L-valinamideHCID 8659660235.4%

Reaction Steps

A solution of N,β,β-trimethyl-L-phenylalanyl-N1-[(1S,2E)-3-(ethoxysulfonyl)-1-isopropylprop-2-enyl]-N1,3-dimethyl-L-valinamide (30 mg, 0.057 mmol) from Example 63 in acetone (1 mL) is treated with tetrabutylammonium iodide (21 mg, 0.057 mmol). The reaction mixture is refluxed for 9 h, and then stirred at room temperature overnight. The solvent is removed. The residue is purified by reversal phase HPLC (mobile phase A: 0.1% TFA/5% acetonitrile/H2O, mobile phase B: 100% acetonitrile) to give 10 mg (28%) of the title compound as a white solid. HRMS (ESI) calcd for C25H41N3O5S [M+H] 496.2840, found 498.2840.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07626023B2
Source datasetuspto-grants-2009_12
ORD IDord-141c7875a12d4a97b4bc603365ed001b
Source noteuspto-grants-2009_12