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Phosphorus oxychloride → 6-Butyl-4-chloro-2-methyl-5-[(4-iodophenyl)methyl]pyrimidine

HRID 1110054
ノート
印刷プレビュー

反応式

HRID 1110054 の反応式
[CH2:1]([C:5]1[N:10]=[C:9]([CH3:11])[NH:8][C:7](=O)[C:6]=1[CH2:13][C:14]1[CH:19]=[CH:18][C:17]([I:20])=[CH:16][CH:15]=1)[CH2:2][CH2:3][CH3:4].O=P(Cl)(Cl)[Cl:23]>>[CH2:1]([C:5]1[N:10]=[C:9]([CH3:11])[N:8]=[C:7]([Cl:23])[C:6]=1[CH2:13][C:14]1[CH:19]=[CH:18][C:17]([I:20])=[CH:16][CH:15]=1)[CH2:2][CH2:3][CH3:4]
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 24813Phosphorus oxychloride2 回HCID 1360140486-Butyl-2-methyl-5-[(4-iodophenyl)methyl]pyrimidine-4(3H)-one

生成物 1

HCID 190187956-Butyl-4-chloro-2-methyl-5-[(4-iodophenyl)methyl]pyrimidine収率 75%

実験手順

A solution of 485 mg (1.27 mmol) 6-butyl-2-methyl-5-[(4-iodophenyl)methyl]pyrimidine-4(3H)-one in 7 mL POCl3 was refluxed for 60 minutes. After cooling to room temperature, excess POCl3 was stripped off in vacuo. The crude product was partitioned between CH2Cl2 and a mixture of brine and NaHCO3. The organic layer was removed and the aqueous layer was extracted three more times with CH2Cl2. The combined organic material was dried over MgSO4, stripped of solvent in vacuo, then was medium pressure chromatographed on silica gel using 10% EtOAc/hexane to give 380 mg of 6-butyl-4-chloro-2-methyl-5-[(4-iodophenyl)methyl]pyrimidine, 75% yield.

後処理

  1. customThe crude product was partitioned between CH2Cl2
  2. additiona mixture of brine and NaHCO3
  3. customThe organic layer was removed
  4. extractionthe aqueous layer was extracted three more times with CH2Cl2
  5. dry with materialThe combined organic material was dried over MgSO4
  6. customchromatographed on silica gel using 10% EtOAc/hexane

出典と根拠

ORDレコード
ord-e3507e334f0847d8a2ab4420fa23ceaf
出典データセット
uspto-grants-1994_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05324729

反応ノート

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