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HRID 24972作成日:2026年10月24日

2,2'-Dipyridyl disulfide → HCID 178443924、化合物

https://huagongshe.com/ja/reaction/24972

反応式

関与物質

役割名称HCID仕込み量
反応物2,2'-Dipyridyl disulfideHCID 65093—
反応物DiisopropylethylamineHCID 81531—
反応物2-IminothiolaneHCID 433941—
反応物Cholesterol EthylenediamineHCID 69752158—
反応物Cholesterol ethylenediamine 2,2'-dipyridyldisulfideHCID 131723204—
溶媒MethanolHCID 887—
溶媒DichloromethaneHCID 6344—
生成物HCID 178443924HCID 178443924—

反応手順

Pure cholesterol-ethylenediamine (10 mmol) was dissolved in 300 mL of DCM. 100 mmol of 2,2′-dipyridyl disulfide was dissolved in 100 mL of methanol and added to the cholesterol-ethylenediamine solution plus 20 mmol of diisopropylethylamine. 15 mmol of 2-iminothiolane was dissolved in 50 mL of methanol and then drop-wise added to the cholesterol-ethylenediamine/2,2′-dipyridyldisulfide solution over 30 minutes at R.T. Following an overnight R.T. stir, organic solvent was roto-evaporated away using medium vacuum until a minimal sample volume remained. Approximately 800 mL of acetonitrile was added to precipitate the crude product. The solid was then collected by filtration onto a Whatman #5 filter apparatus, rinsed several times with acetonitrile and then air-dried. The crude solid was dissolved in a minimal volume of chloroform and chromatographically purified using a silica column. The purified product presented a single TLC spot (4:1 chloroform/methanol), and a single peak (parent ion M+H=685) was identified by positive mode electrospray.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06858226B2
出典データセットuspto-grants-2005_02
ORD IDord-8f7ab44c45384625abf6313842637ab3
出典メモuspto-grants-2005_02