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Benzoyl chloride → HCID 178523928, 화합물

HRID 2063155
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HRID 2063155 반응식
[OH:1][C:2]1[C:3]([C:8]([NH2:10])=[O:9])=[N:4][CH:5]=[CH:6][N:7]=1.C(N(CC)CC)C.[C:18](Cl)(=[O:25])[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1>O1CCCC1.O.Cl>[C:18]([NH:10][C:8]([C:3]1[C:2]([OH:1])=[N:7][CH:6]=[CH:5][N:4]=1)=[O:9])(=[O:25])[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1
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참가 물질

7

반응물 3

HCID 7412Benzoyl chlorideHCID 8471TriethylamineHCID 178513804HCID 178513804, 화합물

생성물 1

HCID 178523928HCID 178523928, 화합물

시약·촉매·용매 3

HCID 313Hydrochloric Acid용매HCID 962Water용매HCID 8028
Tetrahydrofuran
용매

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온도
60 °C

실험 절차

In 50 mL of tetrahydrofuran is suspended 1.00 g of 3-hydroxy-2-pyrazinecarboxamide. Then, 3.5 mL of triethylamine and 1.67 mL of benzoyl chloride are successively added thereto. The resulting solution is stirred at 60° C. for 5 hours and cooled. The deposited crystals are collected by filtration. The crystals thus obtained are suspended in a mixture of 8 mL of water and 1 mL of 1 mol/mL hydrochloric acid, stirred at ambient temperature for 30 minutes, and collected by filtration to obtain 0.41 g of N2-benzoyl-3-hydroxy-2-pyrazinecarboxamide.

후처리

  1. temperaturecooled
  2. filtrationThe deposited crystals are collected by filtration
  3. customThe crystals thus obtained
  4. stirringstirred at ambient temperature for 30 minutes
  5. filtrationcollected by filtration

출처 및 근거

ORD 기록
ord-20f8595587fc46b8bcdd7b88920b3e5a
출처 데이터셋
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
USRE043748E1

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