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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 133818Generated: October 31, 2026

HCID 11504791, compound → HCID 86596603, compound

https://huagongshe.com/reaction/133818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 11504791HCID 11504791—
CatalystTetrabutylammonium IodideHCID 67553—
SolventAcetoneHCID 180—
ProductHCID 86596603HCID 8659660328%
ProductHCID 86596604HCID 86596604—

Reaction Steps

A solution of N,β,β-trimethyl-L-phenylalanyl-N1-[(1S,2E)-3-(ethoxysulfonyl)-1-isopropylbut-2-enyl]-N1,3-dimethyl-L-valinamide (30 mg, 0.046 mmol, from Example 65) in acetone (2 mL) is treated with tetrabutylammonium iodide (20 mg, 0.055 mmol). The reaction mixture is refluxed for 7 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 12 mg (28%) of N,β,β-trimethyl-L-phenylalanyl-N1-[(1S,2E)-1-isopropyl-3-sulfobut-2-enyl] N1,3-dimethyl-L-valinamide as a white solid and 2 mg of N,β,β-trimethyl-L-phenylalanyl-N1-[(1S,2Z)-1-isopropyl-3-sulfobut-2-enyl]-N1,3-dimethyl-L-valinamide

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07390910B2
Source datasetuspto-grants-2008_06
ORD IDord-21e3216e0b7b40e78b0d39403b21cfb5
Source noteuspto-grants-2008_06