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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Trifluoroacetic anhydride → Tetrahydropyridino[1,2-c][1,2,3]oxadiazolone

HRID 2216564
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인쇄 미리보기

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HRID 2216564 반응식
FC(F)(F)C(OC(=O)C(F)(F)F)=O.[N:14]([N:16]1[CH2:21][CH2:20][CH2:19][CH2:18][CH:17]1[C:22]([OH:24])=[O:23])=O>C1COCC1>[NH:14]1[N:16]2[CH2:21][CH2:20][CH2:19][CH2:18][CH:17]2[C:22](=[O:23])[O:24]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 9845Trifluoroacetic anhydrideHCID 20614N-Nitrosopipecolic acid

생성물 1

HCID 69656246Tetrahydropyridino[1,2-c][1,2,3]oxadiazolone

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
0 °C

실험 절차

Trifluoroacetic anhydride (1.93 g) was added to the THF (92 mL) solution of crude (2RS)-1-nitrosopiperidine-2-carboxylic acid under a nitrogen atmosphere at 0° C. and stirred for 5 h at 0° C. and for 2 h at room temperature. The solution was concentrated under a reduced pressure. The residue was applied to silica gel column chromatography, then the column was eluted with n-hexane-AcOEt (1/1–0/1). The titled compound was obtained as colorless crystals (1.10 g, 33%).

후처리

  1. concentrationThe solution was concentrated under a reduced pressure
  2. washthe column was eluted with n-hexane-AcOEt (1/1–0/1)

출처 및 근거

ORD 기록
ord-9ff03be4fa564273b043f6d90e3253ea
출처 데이터셋
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07112582B2

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