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Benzylamine → 2-Benzyl-2,7-diaza-spiro[4.5]decan-6-one

HRID 656472
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인쇄 미리보기

반응식

HRID 656472 반응식
CS(O[CH2:6][CH2:7][C:8]1([CH2:15]OS(C)(=O)=O)[CH2:13][CH2:12][CH2:11][NH:10][C:9]1=[O:14])(=O)=O.[CH2:21]([NH2:28])[C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1>O1CCOCC1.COC(C)(C)C>[CH2:21]([N:28]1[CH2:6][CH2:7][C:8]2([CH2:13][CH2:12][CH2:11][NH:10][C:9]2=[O:14])[CH2:15]1)[C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 7504BenzylamineHCID 86629997Methanesulphonic acid 3-(2-methanesulphonyloxy-ethyl)-2-oxo-piperidin-3-ylmethyl ester

생성물 1

HCID 685748222-Benzyl-2,7-diaza-spiro[4.5]decan-6-one

시약·촉매·용매 2

HCID 15413tert-Butyl methyl ether용매HCID 312751,4-Dioxane용매

실험 절차

A solution of 1 mmol of methanesulphonic acid 3-(2-methanesulphonyloxy-ethyl)-2-oxo-piperidin-3-ylmethyl ester and 3 mmol of benzylamine in 5 ml of dioxane is heated at 60° C. for 30 hours. The reaction mixture is diluted with tert-butyl methyl ether and washed with brine. The organic phase is dried with sodium sulphate and evaporated. From the residue the title compound is identified by means of flash chromatography (SiO2 60 F) on the basis of the Rf value.

후처리

  1. washwashed with brine
  2. dry with materialThe organic phase is dried with sodium sulphate
  3. customevaporated

출처 및 근거

ORD 기록
ord-82cb8e3c82dd468f9fe5f1d767d0b0d2
출처 데이터셋
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08071773B2

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