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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1982357Generated: October 27, 2026

1,2-Dichloroethane → Ac-Pro-Leu-Gly-S-Leu-Leu-Gly-OC2H5

https://huagongshe.com/reaction/1982357

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantAc-Pro-Leu-Gly-OHHCID 7408272—
ReactantHS-Leu-Leu-Gly-OC2H5HCID 131714519—
SolventDimethylformamideHCID 6228—
ProductAc-Pro-Leu-Gly-S-Leu-Leu-Gly-OC2H5HCID 9197786473%

Reaction Steps

To a solution of Ac-Pro-Leu-Gly-OH (0.7 g, 2.1 mmol), HS-Leu-Leu-Gly-OC2H5 (0.6 g, 1.7 mmol) and HBT (0.26 g, 1.7 mmol) in 15 ml dimethylformamide was added EDC (0.4 g, 2.1 mmol). The solution was stirred at room temperature overnight. The solvent was removed in vacuo and the residue partitioned between salt water and ethyl acetate. The ethyl acetate layer was washed consecutively with dilute sodium bicarbonate in salt (NaCl) water, dilute hydrochloric acid in salt water, salt water, 1.0 mM cupric sulfate in salt water (to remove any mercapto products) and finally salt water. The ethyl acetate was dried over magnesium sulfate. The magnesium sulfate was removed by filtration and the filtrate concentrated in vacuo, yielding 0.8 g (73%) glassy residue of crude thiopeptolide product. A 100 mg sample of this crude product was purified by low pressure C18 column chromatography. The purified thiopeptolide, had an acceptable amino acid analysis, a consistent mass spectrum and a single peak on HPLC analysis. Anal. Calcd. for

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04596675
Source datasetuspto-grants-1986_06
ORD IDord-8fa166e3b761425da88ac76728f44136
Source noteuspto-grants-1986_06