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Hydrochloric Acid → HCID 974966, 화합물

HRID 703123
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HRID 703123 반응식
[F:1][C:2]1[CH:15]=[CH:14][CH:13]=[CH:12][C:3]=1[C:4]([NH:6][NH:7][C:8]([NH:10][CH3:11])=[S:9])=O.Cl.N1C=CC=CC=1.C([O-])(O)=O.[Na+].Cl>>[F:1][C:2]1[CH:15]=[CH:14][CH:13]=[CH:12][C:3]=1[C:4]1[N:10]([CH3:11])[C:8](=[S:9])[NH:7][N:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 313Hydrochloric AcidHCID 516892Sodium BicarbonateHCID 34380302-(2-fluorobenzoyl)-N-methyl-1-hydrazinecarbothioamideHCID 10176127Pyridinium chloride

생성물 1

HCID 974966HCID 974966, 화합물수율 48.1%

실험 절차

1-(2-Fluorobenzoyl)-4-methylthiosemicarbazide (11.3 g, 4.97×10-2 mole) or the aforementioned mixture of the above and pyridine hydrochloride and 1 molar aqueous NaHCO3 (480 ml, 4.80×10-1 mole) were stirred and heated to reflux After refluxing overnight, the reaction was cooled in an ice bath before being acidified by the drop-wise addition of concentrated hydrochloric acid (40 ml, 4.8×10-1 mole). The resulting precipitate was collected by filtration, washed with a little H2O, and dried by suction. This afforded a colorless powder 5.0 g (48%). This material was of sufficient purity to go on to the next step. If desired this material could be crystallized from EtOAc/hexane affording colorless needles, mp 137°-139° C.

후처리

  1. temperatureheated
  2. temperatureto reflux
  3. temperatureAfter refluxing overnight
  4. temperaturethe reaction was cooled in an ice bath
  5. filtrationThe resulting precipitate was collected by filtration
  6. washwashed with a little H2O
  7. customdried by suction

출처 및 근거

ORD 기록
ord-1f08e5ec777e4c1484ebea629ce2b430
출처 데이터셋
uspto-grants-1991_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04981863

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