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1,1'-Carbonyldiimidazole → HCID 86694158、化合物

HRID 707290
ノート
印刷プレビュー

反応式

HRID 707290 の反応式
[Br:1][C:2]1[N:7]=[C:6]([NH:8][CH:9]2[CH2:11][CH2:10]2)[C:5]([NH2:12])=[N:4][CH:3]=1.[C:13](N1C=CN=C1)(N1C=CN=C1)=[O:14]>C1COCC1>[Br:1][C:2]1[N:7]=[C:6]2[N:8]([CH:9]3[CH2:10][CH2:11]3)[C:13](=[O:14])[NH:12][C:5]2=[N: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

4

反応物 2

HCID 682631,1'-Carbonyldiimidazole2 回HCID 86694157HCID 86694157、化合物

生成物 1

HCID 86694158HCID 86694158、化合物収率 57%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
66 °C

実験手順

To a heated (50° C.) solution of 6-bromo-N2-cyclopropylpyrazine-2,3-diamine (0.740 g, 3.23 mmol) in THF (20 mL) was added 1,1′-carbonyldiimidazole (1.00 g, 6.17 mmol) in one portion. The reaction was then heated at 66° C. for 3 h. Additional 1,1′-carbonyldiimidazole (1.00 g, 6.17 mmol) was added and the reaction was heated at 50° C. overnight. The reaction was cooled to room temperature and carefully quenched with water (slight exotherm) until gas evolution ceased. The solution was diluted with EtOAc and the layer were separated. The organic layer was washed with water (1×) and brine (1×). The solution was evaporated onto silica gel and purified by flash chromatography (ISCO(40 gram)) eluting with EtOAc:hexanes (0:1→2:3) to give 467 mg (57%) of a yellow crystalline solid. ESI MS 256.9 [M+1].

後処理

  1. temperaturethe reaction was heated at 50° C. overnight
  2. temperatureThe reaction was cooled to room temperature
  3. customcarefully quenched with water (slight exotherm) until gas evolution
  4. additionThe solution was diluted with EtOAc
  5. customthe layer were separated
  6. washThe organic layer was washed with water (1×) and brine (1×)
  7. customThe solution was evaporated onto silica gel
  8. custompurified by flash chromatography (ISCO(40 gram))
  9. washeluting with EtOAc:hexanes (0:1→2:3)

出典と根拠

ORDレコード
ord-0a13f5e878134c1787c7117981ee1b8c
出典データセット
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09174992B2

反応ノート

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