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Hydrochloric Acid → HCID 178508042、化合物

HRID 547383
ノート
印刷プレビュー

反応式

HRID 547383 の反応式
[NH2:1][C:2]1[C:7]([NH:8][C:9](=[O:18])[O:10][CH2:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[CH:6][CH:5]=[CH:4][N:3]=1.ClC1C=CC=C(C(OO)=[O:27])C=1.Cl>CC(C)=O>[NH2:1][C:2]1[C:7]([NH:8][C:9](=[O:18])[O:10][CH2:11][C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=2)=[CH:6][CH:5]=[CH:4][N+:3]=1[O-:27]
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 313Hydrochloric AcidHCID 70297m-Chloroperbenzoic acidHCID 13451701Benzyl (2-aminopyridin-3-yl)carbamate

生成物 1

HCID 178508042HCID 178508042、化合物

試薬・触媒・溶媒 1

HCID 180Acetone溶媒2 回

実験手順

To a solution of benzyl (2-aminopyridin-3-yl)carbamate in acetone was added a solution of m-chloro perbenzoic acid in acetone and the suspension was stirred at room temperature. After 2 hours the suspension was cooled to 0° C., HCl (2N in Et2O) was added, and the precipitate filtered. To the precipitate was added saturated aqueous NaHCO3, EtOAc and MeOH and the mixture stirred until dissolution. The solution was evaporated and the residue washed with water until the pH of the filtrate was neutral. The solid was dried under vacuum.

後処理

  1. temperatureAfter 2 hours the suspension was cooled to 0° C.
  2. filtrationthe precipitate filtered
  3. additionTo the precipitate was added saturated aqueous NaHCO3, EtOAc and MeOH
  4. stirringthe mixture stirred until dissolution
  5. customThe solution was evaporated
  6. washthe residue washed with water until the pH of the filtrate
  7. customThe solid was dried under vacuum

出典と根拠

ORDレコード
ord-4b8f859f683c49b9ad974d223eaa024d
出典データセット
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07939537B2

反応ノート

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