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Ammonia → 2-Ethylthiazolo[4,5-c]quinolin-4-amine

HRID 430538
ノート
印刷プレビュー

反応式

HRID 430538 の反応式
[CH2:1]([C:3]1[S:4][C:5]2[C:14]3[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=3[N:8]=[C:7]([NH:15]C(=O)C(Cl)(Cl)Cl)[C:6]=2[N:22]=1)[CH3:2].N>CO>[CH2:1]([C:3]1[S:4][C:5]2[C:14]3[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=3[N:8]=[C:7]([NH2:15])[C:6]=2[N:22]=1)[CH3:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 222AmmoniaHCID 22648275n-(2-Ethylthiazolo[4,5-c]quinolin-4-yl)trichloroacetamide

生成物 1

HCID 99646202-Ethylthiazolo[4,5-c]quinolin-4-amine

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

N-(2-ethylthiazolo[4,5-c]quinolin-4-yl)trichloroacetamide (0.40 g) was suspended in a solution of ammonia in methanol (20 mL of 2M) and then stirred at ambient temperature for 30 minutes. The reaction mixture was concentrated under vacuum. The residue was washed with water and then dried to provide 0.19 g of crude product which was recrystallized from ethyl acetate/hexane to provide 2-ethylthiazolo[4,5-c]quinolin-4-amine as tan needles, m.p. 170-172° C. Analysis: Calculated for C12H11N3S: % C, 62.85; % H, 4.83; % N, 18.32; Found: % C, 62.58; % H, 4.78; % N, 18.08.

後処理

  1. concentrationThe reaction mixture was concentrated under vacuum
  2. washThe residue was washed with water
  3. customdried
  4. customto provide 0.19 g of crude product which
  5. customwas recrystallized from ethyl acetate/hexane

出典と根拠

ORDレコード
ord-23464d3d232442c5ac179adf4d17a0c7
出典データセット
uspto-grants-2001_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06323200B1

反応ノート

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