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HRID 376425作成日:2026年10月25日

2,3-Bis[(9Z)-9-octadecen-1-yloxy]-1-propanol → 3-O-(2-dimethylaminoethyl)sulfamoyl-1,2-O-dioleylglycerol

https://huagongshe.com/reaction/376425

反応式

関与物質

役割名称HCID仕込み量
反応物2,3-Bis[(9Z)-9-octadecen-1-yloxy]-1-propanolHCID 5380343—
反応物(2-Dimethylaminoethyl)sulfamoyl chlorideHCID 19361100—
溶媒DichloromethaneHCID 6344—
溶媒Pyridine methylene chlorideHCID 21875418—
生成物3-O-(2-dimethylaminoethyl)sulfamoyl-1,2-O-dioleylglycerolHCID 8675186218.3%

反応手順

In 4 ml of methylene chloride-pyridine (2:1) was dissolved 150 mg (0.25 mmol) of 1,2-O-dioleylglycerol. Then, 1 ml of a solution of 150 mg (0.75 mmol) (2-dimethylaminoethyl)sulfamoyl chloride in methylene chloride was added and the reaction was carried out at ambient temperature for 2 hours. After completion of the reaction, the solvent was distilled off under reduced pressure and the residue was treated with methylene chloride-saturated aqueous sodium hydrogen carbonate solution. The methylene chloride layer was dried over sodium sulfate and concentrated under reduced pressure. The residue was subjected to column chromatography (silica gel/methylene chloride-methanol) to provide 34 mg (18%) of the title compound of the invention.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06020317
出典データセットuspto-grants-2000_02
ORD IDord-88f5d475501241098154bbe215df8e61
出典メモuspto-grants-2000_02