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

HRID 373962
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인쇄 미리보기

반응식

HRID 373962 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24813Phosphorus oxychloride2회HCID 1360140486-Butyl-2-methyl-5-[(4-iodophenyl)methyl]pyrimidine-4(3H)-one

생성물 1

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

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-558004552347448b94808c02e829812d
출처 데이터셋
uspto-grants-1992_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05166206

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