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Benzyl Alcohol → HCID 178508946、化合物

HRID 2081799
ノート
印刷プレビュー

反応式

HRID 2081799 の反応式
[Na].[CH2:2]([OH:9])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.Cl[C:11]1[C:12]2[NH:20][N:19]=[N:18][C:13]=2[N:14]=[C:15]([NH2:17])[N:16]=1>O>[C:3]1([CH2:2][O:9][C:11]2[C:12]3[NH:20][N:19]=[N:18][C:13]=3[N:14]=[C:15]([NH2:17])[N:16]=2)[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 244Benzyl AlcoholHCID 5360545Sodium2 回HCID 178508438HCID 178508438、化合物

生成物 1

HCID 178508946HCID 178508946、化合物収率 61.4%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

Sodium metal (3.7 g, 0.162 mol) was added in pieces to benzyl alcohol (117 ml, 1.13 mol) under nitrogen over 20 minutes. The reaction was then heated to 80° for 90 minutes. All of the sodium metal dissolved, and the reaction was left at room temperature for 16 hours. 7-Chloro-1H-1,2,3triazolo[4,5-d]pyrimidin-5-amine (9.23 g. 0.0541 mol) was then added, and the reaction was heated to 60° for 5 hours. The reaction was cooled and left at 5° for 16 hours. Water (500 ml) was added to dissolve the precipitate and then the mixture was extracted with ether (3×200 ml). The pH of the water layer was lowered to 7.0 with concentrated HCl and then to 5.5 with 1N HCl. The precipitate was filtered and dried at room temperature over P2O5 in vacuo to give 8.05 g of desired product.

後処理

  1. temperatureThe reaction was then heated to 80° for 90 minutes
  2. temperaturethe reaction was heated to 60° for 5 hours
  3. temperatureThe reaction was cooled
  4. waitleft at 5° for 16 hours
  5. dissolutionto dissolve the precipitate
  6. extractionthe mixture was extracted with ether (3×200 ml)
  7. filtrationThe precipitate was filtered
  8. dry with materialdried at room temperature over P2O5 in vacuo

出典と根拠

ORDレコード
ord-835c9b615e6249538ba00176c0114b24
出典データセット
uspto-grants-1993_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05185459

反応ノート

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