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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Trifluoroacetic acid → (9aR)-Hexahydropyrazino[2,1-c][1,4]oxazin-4(3H)-one

HRID 2066531
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HRID 2066531 반응식
C(OC([N:8]1[CH2:17][CH2:16][N:15]2[C@@H:10]([CH2:11][O:12][CH2:13][C:14]2=[O:18])[CH2:9]1)=O)(C)(C)C.C(O)(C(F)(F)F)=O>C(Cl)Cl>[CH2:11]1[C@H:10]2[CH2:9][NH:8][CH2:17][CH2:16][N:15]2[C:14](=[O:18])[CH2:13][O:12]1
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참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 58117095HCID 58117095, 화합물

생성물 1

HCID 16124470(9aR)-Hexahydropyrazino[2,1-c][1,4]oxazin-4(3H)-one수율 76%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of (R)-4-oxo-hexahydro-pyrazino[2,1-c][1,4]oxazine-8-carboxylic acid tert-butyl ester in DCM (5 mL) was added TFA (1 mL). The resulting mixture was stirred at RT for 2 h then concentrated in vacuo. The resulting residue was azeotroped with toluene then purified by SCX column to give the title compound as a colourless oil (60 mg, 76%).

후처리

  1. concentrationthen concentrated in vacuo
  2. customThe resulting residue was azeotroped with toluene
  3. customthen purified by SCX column

출처 및 근거

ORD 기록
ord-982ec4c61c4247c188d73c7fc6dbefaf
출처 데이터셋
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08293735B2

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