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Methanol → N-(5-(methoxymethyl)pyridin-2-yl)-5-thiocyanatothiazol-2-amine

HRID 1685346
ノート
印刷プレビュー

反応式

HRID 1685346 の反応式
[S:1]([C:4]1[S:8][C:7]([NH:9][C:10]2[N:15]=[CH:14][C:13]([CH2:16][OH:17])=[CH:12][CH:11]=2)=[N:6][CH:5]=1)[C:2]#[N:3].[CH3:18]O>O=P(Cl)(Cl)Cl>[CH3:18][O:17][CH2:16][C:13]1[CH:12]=[CH:11][C:10]([NH:9][C:7]2[S:8][C:4]([S:1][C:2]#[N:3])=[CH:5][N:6]=2)=[N:15][CH:14]=1
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 887MethanolHCID 59200341HCID 59200341、化合物

生成物 1

HCID 59200492N-(5-(methoxymethyl)pyridin-2-yl)-5-thiocyanatothiazol-2-amine

試薬・触媒・溶媒 1

HCID 24813Phosphorus oxychloride溶媒

反応条件

温度
85 °C

実験手順

(6-(5-Thiocyanatothiazol-2-ylamino)pyridin-3-yl)methanol (0.094 g, 0.356 mmol) was dissolved in POCl3 (3 mL) and the reaction was heated at 85° C. for 3 hours. POCl3 was then evaporated and the resulting oil was washed with water to give a gummy solid. Methanol (10 mL) was added to the solid and the resulting suspension was stirred at 23° C. for over a month. Methanol was evaporated to almost dryness and water was added to precipitate the oil. The resulting solid was filtered and dried under vacuum to give the crude title material (0.109 g, quant.) which was used as such in the next reaction. HPLC ret. time (Condition A): 1.603 min. LC/MS (M+H)+: 279.

後処理

  1. customPOCl3 was then evaporated
  2. washthe resulting oil was washed with water
  3. customto give a gummy solid
  4. customMethanol was evaporated to almost dryness and water
  5. additionwas added
  6. customto precipitate the oil
  7. filtrationThe resulting solid was filtered
  8. customdried under vacuum

出典と根拠

ORDレコード
ord-f344b13b91de4f64ac8cf47837cca926
出典データセット
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08148400B2

反応ノート

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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