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Thiophosgene → HCID 18465370, 화합물

HRID 1416906
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HRID 1416906 반응식
[NH2:1][C:2]1[C:11]([CH3:12])=[C:10]2[C:5]([CH:6]=[CH:7][CH:8]=[N:9]2)=[C:4]([F:13])[CH:3]=1.[C:14](Cl)(Cl)=[S:15].[OH-].[Na+]>O.Cl>[F:13][C:4]1[CH:3]=[C:2]([N:1]=[C:14]=[S:15])[C:11]([CH3:12])=[C:10]2[C:5]=1[CH:6]=[CH:7][CH:8]=[N:9]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 10040Thiophosgene2회HCID 14798Sodium HydroxideHCID 18465378HCID 18465378, 화합물

생성물 1

HCID 18465370HCID 18465370, 화합물

시약·촉매·용매 2

HCID 313Hydrochloric Acid용매HCID 962Water용매

실험 절차

A mixture of 7-amino-5-fluoro-8-methylquinoline (0.39 g) and thiophosgene (0.2 mL) in water (5 mL) and 1N hydrochloric acid (5 mL) is stirred at room temperature for 1.5 hours. An additional amount of thiophosgene (0.1 mL) is added and the mixture stirred another hour. The mixture is treated with 1N sodium hydroxide (25 mL) and extracted with methylene chloride (4×50 mL). The combined extracts are dried over sodium sulfate and rotary evaporated. The residue is purified by flash chromatography on silica gel, eluting with 15% ethyl acetate/hexanes, to afford 5-fluoro-7-isothiocyanato-8-methylquinoline as a tan solid.

후처리

  1. stirringthe mixture stirred another hour
  2. extractionextracted with methylene chloride (4×50 mL)
  3. dry with materialThe combined extracts are dried over sodium sulfate and rotary evaporated
  4. customThe residue is purified by flash chromatography on silica gel
  5. washeluting with 15% ethyl acetate/hexanes

출처 및 근거

ORD 기록
ord-c45bcae1c3e347af95c7ed4a9582e1f0
출처 데이터셋
uspto-grants-1999_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05916900

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