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

Sodium Iodide → (s)-4,6-Diiodo-n-(1-methoxypropan-2-yl)pyrimidin-2-amine

HRID 2056717
노트
인쇄 미리보기

반응식

HRID 2056717 반응식
Cl[C:2]1[CH:7]=[C:6](Cl)[N:5]=[C:4]([NH:9][C@@H:10]([CH3:14])[CH2:11][O:12][CH3:13])[N:3]=1.[IH:15].[I-:16].[Na+].C(Cl)Cl>CCOC(C)=O>[I:15][C:2]1[CH:7]=[C:6]([I:16])[N:5]=[C:4]([NH:9][C@@H:10]([CH3:14])[CH2:11][O:12][CH3:13])[N:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 5238Sodium IodideHCID 6344DichloromethaneHCID 24841Hydrogen iodideHCID 58612018(s)-4,6-Dichloro-n-(1-methoxypropan-2-yl)pyrimidin-2-amine

생성물 1

HCID 58612049(s)-4,6-Diiodo-n-(1-methoxypropan-2-yl)pyrimidin-2-amine

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

실험 절차

A mixture of (S)-4,6-dichloro-N-(1-methoxypropan-2-yl)pyrimidin-2-amine (260 mg, 0.11 mmol, Example 122(a)), hydriodic acid (57 wt. % in water, 40.4 μl, 0.165 mmol, Aldrich), sodium iodide (248 mg, 0.165 mmol) and DCM (5 mL) was stirred at room temperature for 2 h. The reaction mixture was diluted with EtOAc (50 mL), washed with 1N NaOH (2×25 mL) and brine (60 mL), dried over Na2SO4 and filtered. The filtrate was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (7% EtOAc/hexane) to give the title compound. MS (ESI, pos. ion) m/z: 420 (M+1).

후처리

  1. washwashed with 1N NaOH (2×25 mL) and brine (60 mL)
  2. dry with materialdried over Na2SO4
  3. filtrationfiltered
  4. customThe filtrate was evaporated under reduced pressure
  5. customthe residue was purified by silica gel column chromatography (7% EtOAc/hexane)

출처 및 근거

ORD 기록
ord-af99575d338e4b58b4be78405911ee49
출처 데이터셋
uspto-grants-2008_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07335672B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트