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Cyclopropanecarbonyl chloride → HCID 178429156、化合物

HRID 591234
ノート
印刷プレビュー

反応式

HRID 591234 の反応式
[NH2:1][C:2]1[N:7]([NH2:8])[C:6](=[O:9])[CH:5]=[C:4]([CH3:10])[N:3]=1.[CH:11]1([C:14](Cl)=O)[CH2:13][CH2:12]1>O1CCOCC1.CN(C)C=O>[CH:11]1([C:14]2[N:1]=[C:2]3[N:3]=[C:4]([CH3:10])[CH:5]=[C:6]([OH:9])[N:7]3[N:8]=2)[CH2:13][CH2:12]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 2

HCID 77637Cyclopropanecarbonyl chlorideHCID 9131753-Amino-2-imino-6-methyl-2,3-dihydropyrimidin-4(1H)-one

生成物 1

HCID 178429156HCID 178429156、化合物

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide溶媒HCID 312751,4-Dioxane溶媒

実験手順

To a solution of Intermediate 1 (0.5 g, 3.57 mmol) in a mixture of 1,4-dioxane (4 mL) and N,N-dimethylformamide (1 mL), cyclopropanecarbonyl chloride (ALDRICH, 0.49 mL, 5.35 mmol) was added and the resulting mixture was heated under reflux overnight. The reaction was then concentrated under vacuum yielding a pale yellow solid which was purified by flash chromatography (Si, eluting with DCM:MeOH mixtures, gradient from 100:0% to 90:10%) to yield a beige solid which was re-purified by flash chromatography (Si, eluting with DCM:MeOH mixtures from 100:0 to 85:15%). The title compound was obtained as a white solid.

後処理

  1. additionwas added
  2. temperaturethe resulting mixture was heated
  3. temperatureunder reflux overnight
  4. concentrationThe reaction was then concentrated under vacuum
  5. customyielding a pale yellow solid which
  6. customwas purified by flash chromatography (Si, eluting with DCM:MeOH mixtures, gradient from 100:0% to 90:10%)
  7. customto yield a beige solid which
  8. customwas re-purified by flash chromatography (Si, eluting with DCM:MeOH mixtures from 100:0 to 85:15%)

出典と根拠

ORDレコード
ord-40d22c08f45947ff8cae76d78e12cea5
出典データセット
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09238653B2

反応ノート

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