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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Trifluoroacetic acid → 6-Bromo-2-(4-piperidinyl)-1,8-naphthyridine

HRID 580906
노트
인쇄 미리보기

반응식

HRID 580906 반응식
C([N:8]1[CH2:13][CH2:12][CH:11]([C:14]2[CH:23]=[CH:22][C:21]3[C:16](=[N:17][CH:18]=[C:19]([Br:24])[CH:20]=3)[N:15]=2)[CH2:10][CH2:9]1)(OC(C)(C)C)=O.C(O)(C(F)(F)F)=O>C(Cl)Cl>[Br:24][C:19]1[CH:20]=[C:21]2[C:16](=[N:17][CH:18]=1)[N:15]=[C:14]([CH:11]1[CH2:12][CH2:13][NH:8][CH2:9][CH2:10]1)[CH:23]=[CH:22]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 67562152HCID 67562152, 화합물

생성물 1

HCID 675633946-Bromo-2-(4-piperidinyl)-1,8-naphthyridine

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A solution of bromide 3-4 (3.5 g, 8.92 mmol), CH2Cl2 (20 ml) and TFA (10 ml) was stirred for 1.0 h. The reaction was concentrated and then azeotroped with toluene. The residue was dissolved in 1N NaOH and then extracted with CHCl3. The CHCl3 portion was washed with brine, dried (MgSO4) and concentrated providing amine 3-5 as a brown solid.

후처리

  1. concentrationThe reaction was concentrated
  2. customazeotroped with toluene
  3. dissolutionThe residue was dissolved in 1N NaOH
  4. extractionextracted with CHCl3
  5. washThe CHCl3 portion was washed with brine
  6. dry with materialdried (MgSO4)
  7. concentrationconcentrated

출처 및 근거

ORD 기록
ord-c6d2dd03aec94ef382b84d7c15b896a8
출처 데이터셋
uspto-grants-1999_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05919792

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