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Sodium Hydroxide → HCID 20324959, 화합물

HRID 838852
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HRID 838852 반응식
[CH2:1]([C:5]1[N:10]2[N:11]=[CH:12][CH:13]=[C:9]2[N:8]=[C:7]([CH3:14])[CH:6]=1)[CH:2]([CH3:4])[CH3:3].[Br:15]N1C(=O)CCC1=O.[OH-].[Na+]>C(Cl)(Cl)Cl>[Br:15][C:13]1[CH:12]=[N:11][N:10]2[C:5]([CH2:1][CH:2]([CH3:4])[CH3:3])=[CH:6][C:7]([CH3:14])=[N:8][C:9]=12
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 14798Sodium HydroxideHCID 67184N-bromobutanimideHCID 203249475-Methyl-7-(2-methylpropyl)pyrazolo[1,5-a]pyrimidine

생성물 1

HCID 20324959HCID 20324959, 화합물

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

A solution of 7.5 g (0.026 mol) of 7-isobutyl-5-methylpyrazolo-[1,5-a]pyrimidine in 60 ml chloroform was treated with 4.6 gm (0.026 mol) of N-bromosuccinimide. The mixture was stirred at ambient temperature and then allowed to cool overnight in the refrigerator. The mixture was then poured over ice (100 gm), rendered alkaline with 6N NaOH, and extracted with chloroform. The chloroform solution was separated, dried (Na2SO4), and distilled to yield 5.5 gm, (47%) of a light yellow, viscous oil, b.p. 127°-129° /1.5 mm.

후처리

  1. temperatureto cool overnight in the refrigerator
  2. extractionextracted with chloroform
  3. customThe chloroform solution was separated
  4. dry with materialdried (Na2SO4)
  5. distillationdistilled
  6. customto yield 5.5 gm, (47%) of a light yellow, viscous oil, b.p. 127°-129° /1.5 mm

출처 및 근거

ORD 기록
ord-13be8c0a0b804772ab19f03deb2a628c
출처 데이터셋
uspto-grants-1978_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04093617

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