ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
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
  1. ホーム
  2. /反応

Hydrochloric Acid → HCID 178434155、化合物

HRID 524918
ノート
印刷プレビュー

反応式

HRID 524918 の反応式
[C:1]([NH:4][NH:5][C:6](=[S:15])[NH:7][C:8]1[CH:13]=[CH:12][N:11]=[CH:10][C:9]=1[Br:14])(=O)[CH3:2].Cl>C(=O)([O-])O.[Na+]>[Br:14][C:9]1[CH:10]=[N:11][CH:12]=[CH:13][C:8]=1[N:7]1[C:1]([CH3:2])=[N:4][N:5]=[C:6]1[SH:15]
参加物反応条件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 313Hydrochloric AcidHCID 86720972HCID 86720972、化合物

生成物 1

HCID 178434155HCID 178434155、化合物収率 81.4%

試薬・触媒・溶媒 1

HCID 516892Sodium Bicarbonate溶媒

反応条件

温度
100 °C

実験手順

2-acetyl-N-(3-bromopyridin-4-yl)hydrazinecarbothioamide (200 mg, 0.6917 mmol) was dissolved in sodium hydrogen carbonate (4 mL,) and stirred at 50° C. for 2 hrs and at 100° C. for 5 hrs. The reaction mixture was then allowed to stand at RT for 48 h before it was carefully neutralised with dilute HCl and partitioned with 10% MeOH in DCM. The aqueous layer was extracted with further 10% MeOH in DCM (3×10 mL) and the combined organics were dried over Na2SO4, filtered and concentrated under reduced pressure to give 4-(3-bromopyridin-4-yl)-5-methyl-4H-1,2,4-triazole-3-thiol as an orange solid (152.6 mg). MS (ES+) 272.9.

後処理

  1. waitto stand at RT for 48 h before it
  2. custompartitioned with 10% MeOH in DCM
  3. extractionThe aqueous layer was extracted with further 10% MeOH in DCM (3×10 mL)
  4. dry with materialthe combined organics were dried over Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-efdbf25eb2604042a8f08df9f8ddaa3e
出典データセット
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09340546B2

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート