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4-Piperidinecarboxylic acid → 5-Bromo-7-fluoro-2-(piperidin-4-yl)benzo[d]oxazole

HRID 710077
노트
인쇄 미리보기

반응식

HRID 710077 반응식
[NH2:1][C:2]1[CH:7]=[C:6]([Br:8])[CH:5]=[C:4]([F:9])[C:3]=1[OH:10].[NH:11]1[CH2:19][CH2:18][CH:14]([C:15](O)=O)[CH2:13][CH2:12]1.[OH-].[Na+]>>[Br:8][C:6]1[CH:5]=[C:4]([F:9])[C:3]2[O:10][C:15]([CH:14]3[CH2:18][CH2:19][NH:11][CH2:12][CH2:13]3)=[N:1][C:2]=2[CH:7]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 37734-Piperidinecarboxylic acidHCID 14798Sodium HydroxideHCID 27376372-Amino-4-bromo-6-fluorophenol

생성물 1

HCID 710895515-Bromo-7-fluoro-2-(piperidin-4-yl)benzo[d]oxazole수율 52.7%

반응 조건

온도
195 °C

실험 절차

2-amino-4-bromo-6-fluorophenol (1.7 g, 8.24 mmol) and isonipecotic acid (1.06 g, 8.24 mmol) were dissolved in polyphosphoric acid (28 g). This mixture was heated to 195° C. for 3 h. After 3 h, reaction mixture cooled to rt and basified with aqueous NaOH solution to pH 14. Solid that obtained was filtered and dried to obtain the title compound (1.3 g) as a brown solid.

후처리

  1. customreaction mixture
  2. customSolid that obtained
  3. filtrationwas filtered
  4. customdried

출처 및 근거

ORD 기록
ord-d6c02776a5a942dfb770966f1de5e44a
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09181214B2

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