N-Iodosuccinimide → 5-Iodo-7H-pyrrolo[2,3-d]pyrimidine

HRID 82243

반응식

HRID 82243 반응식
[N:1]1[C:6]2[NH:7][CH:8]=[CH:9][C:5]=2[CH:4]=[N:3][CH:2]=1.[I:10]N1C(=O)CCC1=O>C(#N)C>[I:10][C:9]1[C:5]2[CH:4]=[N:3][CH:2]=[N:1][C:6]=2[NH:7][CH:8]=1

참가 물질

4

반응물 2

HCID 120273N-IodosuccinimideHCID 2615917H-Pyrrolo(2,3-d)pyrimidine

생성물 1

HCID 106103365-Iodo-7H-pyrrolo[2,3-d]pyrimidine수율 81%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

A mixture of 7H-pyrrolo[2,3-d]pyrimidine (Preparation 202, 28.0 g, 235 mmol) and N-iodosuccinimide (55.4 g, 246 mmol) in acetonitrile (470 mL) was stirred at room temperature for 16 hours. The solids were filtered, rinsed with acetonitrile (150 mL) and dried in vacuo. The solid was dissolved in 1.5 L of 1N aqueous sodium hydroxide solution and to it was added 2N aqueous hydrogen chloride solution until ˜pH 9. The resulting precipitate was filtered, rinsed with water (300 mL), and dried in vacuo for 16 hours at 70° C., ˜10 mbar, to afford the title compound in 81% yield, 46.84 g.

후처리

  1. filtrationThe solids were filtered
  2. washrinsed with acetonitrile (150 mL)
  3. customdried in vacuo
  4. dissolutionThe solid was dissolved in 1.5 L of 1N aqueous sodium hydroxide solution and to it
  5. additionwas added 2N aqueous hydrogen chloride solution until ˜pH 9
  6. filtrationThe resulting precipitate was filtered
  7. washrinsed with water (300 mL)
  8. customdried in vacuo for 16 hours at 70° C.

출처 및 근거

ORD 기록
ord-f409a75c58cd44738a7c6792df30c2bb
출처 데이터셋
uspto-grants-2014_09
특허 번호
US08846698B2

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