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Sodium hydrosulfide hydrate → HCID 178505612, 화합물

HRID 715733
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HRID 715733 반응식
Cl[C:2]1[CH:3]=[CH:4][C:5]2[N:6]([C:8]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=3[F:17])=[N:9][N:10]=2)[N:7]=1.O.[SH-:19].[Na+]>C(O)C>[F:17][C:12]1[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=1[C:8]1[N:6]2[N:7]=[C:2]([SH:19])[CH:3]=[CH:4][C:5]2=[N:10][N:9]=1
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참가 물질

4

반응물 2

HCID 16211346Sodium hydrosulfide hydrateHCID 431443926-chloro-3-(2-fluorophenyl)[1,2,4]triazolo[4,3-b]pyridazine

생성물 1

HCID 178505612HCID 178505612, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A solution of 6-chloro-3-(2-fluorophenyl)-[1,2,4]triazolo[4,3-b]pyridazine (1 mmol) and sodium hydrosulfide hydrate (1.5 equiv.) in ethanol was refluxed for 2-6 hours. The solvent was removed under reduced pressure, water (2 ml) was added, and the pH adjusted to 9 with sodium hydroxide solution. After removing the resulting precipitate, the filtrate was acidified with 6M HCl to a pH of 3, and the formed precipitate was collected, washed with cold water, and dried to give 3-(2-fluorophenyl)-[1,2,4]triazolo[4,3-b]pyridazine-6-thiol. This compound is taken on to the next step without purification

후처리

  1. customThe solvent was removed under reduced pressure, water (2 ml)
  2. additionwas added
  3. customAfter removing the resulting precipitate
  4. customthe formed precipitate was collected
  5. washwashed with cold water
  6. customdried

출처 및 근거

ORD 기록
ord-ee97f53ce6014a88a43a0a894a367fe4
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09187484B2

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