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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 615705Generated: October 29, 2026

Palmitoyl chloride → HCID 20426911, compound

https://huagongshe.com/reaction/615705

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPalmitoyl chlorideHCID 8206—
ReactantHCID 20426898HCID 20426898—
SolventPyridineHCID 1049—
ProductHCID 20426911HCID 2042691134%

Reaction Steps

To 3.0 g. of 4-(4-chlorophenyl)-2-(hydroxymethyl)-5H-pyrido[3,4-b][1,4]benzothiazin-3(2H)-one (8.4 mmol.) suspended in 30 ml. of pyridine at 0° C. was added dropwise 2.5 ml. of hexadecanoyl chloride (10.9 mmol.). After stirring for 45 minutes, the mixture was poured onto ice-water and allowed to stand for 16 hours at room temperature, resulting in the formation of a yellow precipitate. The precipitate was collected, washed with water and air-dried, then purified using flash chromatography on silica gel, using a mixture of 5% ethyl acetate: 95% methylene chloride as the eluent. Fractions containing the product were combined, and the solvent was removed in vacuo. The residue was triturated with diethyl ether to yield 4-(4-chlorophenyl)-2-[(1-oxohexadecyloxy)methyl]-5H-pyrido[3,4-b][1,4]benzothiazin-3(2H)-one as a light yellow solid (1.69 g; 34% yield) having the structural formula, ##STR18## a melting point in the range of 89°-92° C. and the following elemental analysis:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04500708
Source datasetuspto-grants-1985_02
ORD IDord-9b455b3b7f244647a2bc5c466877d153
Source noteuspto-grants-1985_02