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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15108생성일: 2026년 10월 27일

Piperidine-1-propanol → 5-chloro-thiophene-2-carboxylic acid-N-{1-methyl-1-[3-methyl-4-(2-{3-hydroxy-prop-1-yl}-piperidin-1-yl-carbonyl)-phenylcarbamoyl]-ethyl}-amide

https://huagongshe.com/reaction/15108

반응식

참여 물질

역할이름HCID투입량
반응물Piperidine-1-propanolHCID 66032—
반응물DiisopropylethylamineHCID 81531—
반응물O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
반응물4-{2-[(5-Chloro-thiophene-2-carbonyl)-amino]-2-methyl-propionylamino}-2-methyl-benzoic acidHCID 68637770—
용매DimethylformamideHCID 6228—
생성물5-chloro-thiophene-2-carboxylic acid-N-{1-methyl-1-[3-methyl-4-(2-{3-hydroxy-prop-1-yl}-piperidin-1-yl-carbonyl)-phenylcarbamoyl]-ethyl}-amideHCID 58774361—

반응 단계

200 μl of a 0.05 molar solution of 4-{2-[(5-chloro-thiophene-2-carbonyl)-amino]-2-methyl-propionylamino}-2-methyl-benzoic acid, which additionally contains 0.05 mol/l DIPEA, in DMF are combined with 100 μl of a 0.1-molar solution of TBTU in DMF on a microtitre plate and mixed for 10 mins on a shaker. Then 200 μl of a 0,05-molar solution of (3-hydroxy-prop-1-yl)-piperidine, which additionally contains 0.05 mol/l DIPEA, are pipetted in and again mixed in by shaking. After 16 h at ambient temperature the mixture is filtered through basic aluminium oxide and washed with DMF/methanol=9:1. Then it is evaporated down i. vac.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732466B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-1df2cfb453494b1a936f45aad2419613
출처 메모uspto-grants-2010_06