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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrogen Bromide → HCID 178515474, 화합물

HRID 1955587
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HRID 1955587 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([CH:18]=[CH:19][C:20]=1[Cl:21])[CH2:5][N:6]1[C:14]2[C:9](=[CH:10][C:11]([O:15]C)=[CH:12][CH:13]=2)[C:8]([OH:17])=[N:7]1.Br.O.[OH-].[Na+]>C(O)(=O)C>[Cl:1][C:2]1[CH:3]=[C:4]([CH:18]=[CH:19][C:20]=1[Cl:21])[CH2:5][N:6]1[C:14]2[C:9](=[CH:10][C:11]([OH:15])=[CH:12][CH:13]=2)[C:8]([OH:17])=[N:7]1
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참가 물질

6

반응물 4

HCID 260Hydrogen BromideHCID 962WaterHCID 14798Sodium HydroxideHCID 178487266HCID 178487266, 화합물

생성물 1

HCID 178515474HCID 178515474, 화합물

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

4.85 g 1-(3,4-dichlorobenzyl)-5-methoxy-1H-indazole-3-ol are heated in 30 ml acetic acid and 30 ml 50% hydrobromic acid for 4 hours under gentle reflux. After cooling, the mixture is stirred into 250 ml water, rendered alkaline with concentrated sodium hydroxide solution and extracted twice with 80 ml tert-butyl methyl ether. The aqueous phase is acidified with sulfuric acid and extracted by shaking three times with 200 ml tert-butyl methyl ether. The combined ether phases are dried over sodium sulfate and distilled to dryness under vacuum. The residue is washed with a small amount of tert-butyl methyl ether and dried.

후처리

  1. temperatureAfter cooling
  2. extractionextracted twice with 80 ml tert-butyl methyl ether
  3. extractionextracted
  4. dry with materialThe combined ether phases are dried over sodium sulfate
  5. distillationdistilled to dryness under vacuum
  6. washThe residue is washed with a small amount of tert-butyl methyl ether
  7. customdried

출처 및 근거

ORD 기록
ord-e0951522de2d4d14964791f7891de963
출처 데이터셋
uspto-grants-1998_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05776932

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