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Thionyl Chloride → 4-Bromothiazole-2-carbohydrazide

HRID 2170911
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HRID 2170911 반응식
[Br:1][C:2]1[N:3]=[C:4]([C:7]([OH:9])=O)[S:5][CH:6]=1.O=S(Cl)Cl.O.[NH2:15][NH2:16]>CO>[Br:1][C:2]1[N:3]=[C:4]([C:7]([NH:15][NH2:16])=[O:9])[S:5][CH:6]=1
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참가 물질

5

반응물 3

HCID 24386Thionyl ChlorideHCID 24654Hydrazine hydrate (1:1)HCID 151220654-Bromo-1,3-thiazole-2-carboxylic acid

생성물 1

HCID 580356604-Bromothiazole-2-carbohydrazide수율 78.1%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of the 4-bromothiazole-2-carboxylic acid (2.0 g, 9.8 mmol) in MeOH (10 mL) was added SOCl2 (710 μL, 9.8 mmol) and the reaction was refluxed for 3 hours. The reaction was concentrated, the residue was suspended in EtOH (10 mL), hydrazine hydrate (2.4 mL, 49 mmol) was added and the reaction was heated to reflux for 90 minutes. The reaction was concentrated, suspended in CH3CN, filtered, and the solids were washed with CH3CN, Et2O, and dried to afford 1.7 g (77%) of 4-bromothiazole-2-carbohydrazide as a yellow solid. M+1=222.1

후처리

  1. temperaturethe reaction was refluxed for 3 hours
  2. concentrationThe reaction was concentrated
  3. temperaturethe reaction was heated
  4. temperatureto reflux for 90 minutes
  5. concentrationThe reaction was concentrated
  6. filtrationfiltered
  7. washthe solids were washed with CH3CN, Et2O
  8. customdried

출처 및 근거

ORD 기록
ord-0a18f912c896420fa0b5841ba0777e66
출처 데이터셋
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09051313B2

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