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Calcium Carbonate → HCID 178513810、化合物

HRID 392357
ノート
印刷プレビュー

反応式

HRID 392357 の反応式
[OH:1][C:2]1[C:3]([C:8]([NH2:10])=[O:9])=[N:4][CH:5]=[CH:6][N:7]=1.[F:11]F.C(=O)([O-])[O-].[Ca+2]>O>[F:11][C:5]1[N:4]=[C:3]([C:8]([NH2:10])=[O:9])[C:2]([OH:1])=[N:7][CH:6]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 10112Calcium CarbonateHCID 24524Fluorine2 回HCID 178513804HCID 178513804、化合物

生成物 1

HCID 178513810HCID 178513810、化合物

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

In 200 mL of water was suspended 1.0 g of 3-hydroxy-2-pyrazinecarboxamide. At room temperature, 10% fluorine gas (a fluorine gas diluted with nitrogen gas) was introduced at a rate of 45 mL per minute for a period of 25 minutes. Then, nitrogen gas was introduced for 45 minutes, and the liquid reaction mixture was neutralized with calcium carbonate, the deposited precipitate was filtered off, the filtrate was concentrated under reduced pressure, and the solid product thus obtained was purified by silica gel column chromatography [eluent: n-hexane:ethyl acetate=5:1] to obtain 0.008 g of 6-fluoro-3-hydroxy-2-pyrazinecarboxamide as a white-colored solid product.

後処理

  1. additionwas introduced at a rate of 45 mL per minute for a period of 25 minutes
  2. additionThen, nitrogen gas was introduced for 45 minutes
  3. customthe liquid reaction mixture
  4. filtrationthe deposited precipitate was filtered off
  5. concentrationthe filtrate was concentrated under reduced pressure
  6. customthe solid product thus obtained
  7. customwas purified by silica gel column chromatography [eluent: n-hexane:ethyl acetate=5:1]

出典と根拠

ORDレコード
ord-db244f86290d46ee90463e77e2bc6cfb
出典データセット
uspto-grants-2004_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06800629B2

反応ノート

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