돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 272251생성일: 2026년 10월 27일

Tryptamine → HCID 178505055, 화합물

https://huagongshe.com/reaction/272251

반응식

참여 물질

역할이름HCID투입량
반응물TryptamineHCID 1150—
반응물1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물HCID 178505057HCID 178505057—
용매AcetonitrileHCID 6342—
용매DichloromethaneHCID 6344—
용매TriethylamineHCID 8471—
생성물HCID 178505055HCID 178505055—

반응 단계

A solution of 0.3 g (0.45 mmol) of trans-4-[4-(benzyl{(2S)-3-[4-(benzyloxy)-3-[(methylsulfonyl)amino]phenoxy]-2-hydroxypropyl}amino)cyclohexyl]benzoic acid (preparation 3), of 0.78 g (0.91 mmol) of 1-hydroxybenzotriazole, of 0.175 g (0.91 mmol) of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide, of 0.19 ml of triethylamine and of 0.138 g (0.86 mmol) of tryptamine in a mixture of 4 ml of dichloromethane and 0.8 ml of acetonitrile is stirred for 24 h. The solvents are evaporated under reduced pressure. Dichloromethane and water are added and the organic phase is washed three times with water. The organic phases are dried over magnesium sulfate and concentrated under reduced pressure. The title compound is obtained in the form of a white solid (0.246 g, 58%) after purification on silica gel (eluent: heptane/ethyl acetate 60/40 for 10 min, 60/40 to 40/60 in 10 min and then 40/60 for 20 min gradient). [M+H+]=801.6

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07453010B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-ea988d814a9d4954a72630fd61008ae2
출처 메모uspto-grants-2008_11