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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Methanol → HCID 57743038、化合物

HRID 1924320
ノート
印刷プレビュー

反応式

HRID 1924320 の反応式
[Br:1][C:2]1[C:3]([C:11]([OH:13])=[O:12])=[C:4]2[NH:10][CH:9]=[N:8][C:5]2=[N:6][CH:7]=1.OS(O)(=O)=O.[CH3:19]O>>[Br:1][C:2]1[C:3]([C:11]([O:13][CH3:19])=[O:12])=[C:4]2[NH:10][CH:9]=[N:8][C:5]2=[N:6][CH:7]=1
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 3

HCID 887MethanolHCID 1118Sulfuric AcidHCID 20501306-Bromo-3H-imidazo[4,5-B]pyridine-7-carboxylic acid

生成物 1

HCID 57743038HCID 57743038、化合物収率 70%

実験手順

Absolute methanol (30 ml) is added to 6-bromo-1H-imidazo[4,5-b]pyridine-7-carboxylic acid x208 (Zerenex; 2.2 g, 9.1 mmol). Concentrated H2SO4 (4 ml) is added to the obtained suspension at 0° C. The reaction mixture is refluxed under protection from the air moisture and vigorous stirring for 10 h. The reaction mixture is then evaporated to half-volume in the vacuum of a rotary evaporator and neutralized under cooling with ice with aqueous ammonia to pH 8-9. The formed precipitate is quickly separated by filtration, washed with ice-cold water (2×30 ml), and dried over P2O5 at 1 mmHg overnight to afford methyl 6-bromo-1H-imidazo[4,5-b]pyridine-7-carboxylate x209 (1.63 g).

後処理

  1. temperatureThe reaction mixture is refluxed under protection from the air moisture
  2. customThe reaction mixture is then evaporated to half-volume in the vacuum of a rotary evaporator
  3. temperatureunder cooling with ice with aqueous ammonia to pH 8-9
  4. customThe formed precipitate is quickly separated by filtration
  5. washwashed with ice-cold water (2×30 ml)
  6. dry with materialdried over P2O5 at 1 mmHg overnight

出典と根拠

ORDレコード
ord-b7c6506edf7940229365a33061ebab13
出典データセット
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08178533B2

反応ノート

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