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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Formamide → HCID 178435582、化合物

HRID 2190079
ノート
印刷プレビュー

反応式

HRID 2190079 の反応式
[NH2:1][C:2]1[CH2:6][CH2:5][CH:4]([CH2:7][CH3:8])[C:3]=1[C:9]([O:11]C)=O.C([O-])=O.[NH4+].[CH:17]([NH2:19])=O>>[CH2:7]([CH:4]1[C:3]2[C:9]([OH:11])=[N:19][CH:17]=[N:1][C:2]=2[CH2:6][CH2:5]1)[CH3:8]
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 3

HCID 713FormamideHCID 2723923Ammonium formateHCID 68735309Methyl 2-amino-5-ethylcyclopent-1-enecarboxylate

生成物 1

HCID 178435582HCID 178435582、化合物収率 71.9%

反応条件

温度
150 °C

実験手順

Methyl 2-amino-5-ethylcyclopent-1-enecarboxylate (1.62 g, 9.57 mmol) was combined with ammonium formate (3.02 g, 47.9 mmol) and formamide (3.80 mL, 95.7 mmol), and the reaction mixture was heated to 150° C. for 16 hours. Conversion was confirmed by LCMS. The reaction was cooled to room temperature and partitioned between a 5:1 DCM/i-PrOH solution and water. The aqueous layer was extracted multiple times with the same DCM/i-PrOH solution. The combined extracts were concentrated to dryness and partitioned between DCM and brine. The organic portion was concentrated to provide 5-ethyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-ol (1.13 g, 6.88 mmol, 71.9% yield) as an oil, which was taken to the next step without purification. MS (APCI+) [M+H]: 165.0.

後処理

  1. temperatureThe reaction was cooled to room temperature
  2. custompartitioned between a 5:1 DCM/i-PrOH solution and water
  3. extractionThe aqueous layer was extracted multiple times with the same DCM/i-PrOH solution
  4. concentrationThe combined extracts were concentrated to dryness
  5. custompartitioned between DCM and brine
  6. concentrationThe organic portion was concentrated

出典と根拠

ORDレコード
ord-14c60b777cf84335ab7c442ca891c728
出典データセット
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08324221B2

反応ノート

読み込み中…

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