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

HRID 1838811
ノート
印刷プレビュー

反応式

HRID 1838811 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-fece040fd97142688d363a76d14920bd
出典データセット
uspto-grants-2004_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06677334B2

反応ノート

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