HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 615705Generated: October 29, 2026
Palmitoyl chloride → HCID 20426911, compound
https://huagongshe.com/reaction/615705
Participants
| Role | Name | HCID | Charge |
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| Reactant | Palmitoyl chloride | HCID 8206 | — |
| Reactant | HCID 20426898 | HCID 20426898 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 20426911 | HCID 20426911 | 34% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04500708 |
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| Source dataset | uspto-grants-1985_02 |
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| ORD ID | ord-9b455b3b7f244647a2bc5c466877d153 |
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| Source note | uspto-grants-1985_02 |
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