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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 567423Generated: October 26, 2026

Pyridine → Methyl (2R,3S)-3-(9-anthracenesulfonamido)-3-phenyl-2-hydroxypropionate

https://huagongshe.com/reaction/567423

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAnthracene-9-sulfonyl chlorideHCID 15310604—
Reactant(3S)-3-Phenylisoserine methyl esterHCID 21968353—
SolventDichloromethaneHCID 6344—
ProductMethyl (2R,3S)-3-(9-anthracenesulfonamido)-3-phenyl-2-hydroxypropionateHCID 57078772—

Reaction Steps

(3S)-3-Phenylisoserine methyl ester (I, 0.38 g, 1.95 mmol) is dissolved in methylene chloride (5 mL) and pyridine (1 mL) and the solution treated with a suspension of 9-anthracenesulfonylchloride (0.536 g, 1.95 mmol). The reaction is stirred at 23° for 90 min. The reaction is then poured into methylene chloride and extracted with hydrochloric acid (1 N) and aqueous bicarbonate (5%) and dried over magnesium sulfate. Concentration of the organic layer under reduced pressure produces crude product. This concentrate is chromatographed (silica gel 60; ethyl acetate/toluene, 20/80) to give the title compound, TLC (silica gel GF) Rf=0.38 in (ethyl acetate/toluene, 2/8); NMR(CDCl3, TMS) 3.11, 3.57, 4.18, 4.78, 6.22, 6.59, 6.67, 7.50, 7.55-7.75, 7.92, 8.09, 8.47 and 9.15 δ.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06177573B1
Source datasetuspto-grants-2001_01
ORD IDord-7483d01346784f73b0176dc1cc080c68
Source noteuspto-grants-2001_01