홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Isopropyl iodide → 5-Iodo-7-isopropyl-7H-pyrrolo[2,3-d]pyrimidine

HRID 82176
노트
인쇄 미리보기

반응식

HRID 82176 반응식
[I:1][C:2]1[C:10]2[CH:9]=[N:8][CH:7]=[N:6][C:5]=2[NH:4][CH:3]=1.C(=O)([O-])[O-].[Cs+].[Cs+].I[CH:18]([CH3:20])[CH3:19].[Cl-].[NH4+]>CN(C=O)C>[I:1][C:2]1[C:10]2[CH:9]=[N:8][CH:7]=[N:6][C:5]=2[N:4]([CH:18]([CH3:20])[CH3:19])[CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 6362Isopropyl iodideHCID 10796Cesium carbonateHCID 25517Ammonium ChlorideHCID 106103365-Iodo-7H-pyrrolo[2,3-d]pyrimidine

생성물 1

HCID 708171765-Iodo-7-isopropyl-7H-pyrrolo[2,3-d]pyrimidine수율 77%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a mixture of 5-iodo-7H-pyrrolo[2,3-d]pyrimidine (Preparation 201, 2.90 g, 12.0 mmol) and cesium carbonate (5.78 g, 17.8 mmol) in DMF (45 mL) was added 2-iodopropane (1.78 mL, 17.8 mmol). The mixture was stirred at room temperature for 3 hours. The reaction mixture was then poured onto saturated aqueous ammonium chloride (500 mL) and a solid precipitated. The solid was collected by filtration, rinsed with water (200 mL) and dried under reduced pressure for 17 hours to afford the title compound as a brown solid in 77% yield, 2.61 g.

후처리

  1. customa solid precipitated
  2. filtrationThe solid was collected by filtration
  3. washrinsed with water (200 mL)
  4. customdried under reduced pressure for 17 hours

출처 및 근거

ORD 기록
ord-62c92f0c8c86496cb5550895e0d2c83d
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08846698B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트