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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 24972생성일: 2026년 10월 24일

2,2'-Dipyridyl disulfide → HCID 178443924, 화합물

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

반응식

참여 물질

역할이름HCID투입량
반응물2,2'-Dipyridyl disulfideHCID 65093—
반응물DiisopropylethylamineHCID 81531—
반응물2-IminothiolaneHCID 433941—
반응물Cholesterol EthylenediamineHCID 69752158—
반응물Cholesterol ethylenediamine 2,2'-dipyridyldisulfideHCID 131723204—
용매MethanolHCID 887—
용매DichloromethaneHCID 6344—
생성물HCID 178443924HCID 178443924—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06858226B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-8f7ab44c45384625abf6313842637ab3
출처 메모uspto-grants-2005_02