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Sodium hydride → HCID 68181763、化合物

HRID 1398637
ノート
印刷プレビュー

反応式

HRID 1398637 の反応式
[I:1][C:2]1[CH:10]=[C:9]2[C:5]([CH:6]=[N:7][NH:8]2)=[CH:4][CH:3]=1.[H-].[Na+].Cl[C:14]1[N:19]=[CH:18][N:17]=[C:16]([NH2:20])[CH:15]=1>CN(C=O)C>[I:1][C:2]1[CH:10]=[C:9]2[C:5]([CH:6]=[N:7][N:8]2[C:14]2[N:19]=[CH:18][N:17]=[C:16]([NH2:20])[CH:15]=2)=[CH:4][CH:3]=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

5

反応物 3

HCID 24758Sodium hydrideHCID 2380124-Amino-6-chloropyrimidineHCID 129912416-iodo-1H-indazole

生成物 1

HCID 68181763HCID 68181763、化合物収率 35.9%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
60 °C

実験手順

To a solution of 6-iodoindazole (500 mg, 2.05 mmol) in DMF (8 mL) was added NaH (60% oil dispersion, 131.12 mg, 3.28 mmol) at 0° C. The mixture was stirred at 0° C. to RT for 10 minutes before addition of 6-chloropyrimidin-4-amine (477.78 mg, 3.69 mmol) and stirring at 60° C. for 17 hr and then transferred to a pressure tube and heated at 70° C. for a further 6 hr. The reaction mixture was cooled and quenched by the addition of water (10 ml) and EtOAc (a few drops) was added. The resultant precipitate was collected by suction filtration and then thoroughly dried under high vacuum to give the title intermediate (248 mg): LC-MS: m/z=+338.20 (M+H)+.

後処理

  1. customtransferred to a pressure tube
  2. temperatureheated at 70° C. for a further 6 hr
  3. temperatureThe reaction mixture was cooled
  4. customquenched by the addition of water (10 ml) and EtOAc (a few drops)
  5. additionwas added
  6. filtrationThe resultant precipitate was collected by suction filtration
  7. customthoroughly dried under high vacuum

出典と根拠

ORDレコード
ord-8abd5d306d2f495c8d0ad0770f8e0a96
出典データセット
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08901313B2

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