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

Dimethylformamide → 1-Benzyl-6-chloro-2-isopropyl-1H-pyrrolo[3,2-c]pyridine-3-carbaldehyde

HRID 2384500
노트
인쇄 미리보기

반응식

HRID 2384500 반응식
O=P(Cl)(Cl)Cl.[CH2:6]([N:13]1[C:21]2[CH:20]=[C:19]([Cl:22])[N:18]=[CH:17][C:16]=2[CH:15]=[C:14]1[CH:23]([CH3:25])[CH3:24])[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.CN([CH:29]=[O:30])C>>[CH2:6]([N:13]1[C:21]2[CH:20]=[C:19]([Cl:22])[N:18]=[CH:17][C:16]=2[C:15]([CH:29]=[O:30])=[C:14]1[CH:23]([CH3:25])[CH3:24])[C:7]1[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 6228Dimethylformamide2회HCID 24813Phosphorus oxychlorideHCID 580250631-Benzyl-6-chloro-2-isopropyl-1H-pyrrolo[3,2-c]pyridine2회

생성물 1

HCID 580250621-Benzyl-6-chloro-2-isopropyl-1H-pyrrolo[3,2-c]pyridine-3-carbaldehyde

반응 조건

온도
80 °C

실험 절차

POCl3 (0.31 ml, 3.42 mmol) was added to anhydrous DMF (5 ml) at 0° C. slowly and stirred for 20 min. To this solution was added a solution of 1-benzyl-6-chloro-2-isopropyl-1H-pyrrolo[3,2-c]pyridine (Compound 13, 195 mg, 0.68 mmol) in anhydrous DMF (7 ml) at room temperature. The mixture was stirred at room temperature for 2 h and was then heated to 60° C. for 2 h and 80° C. for 0.5 h. The reaction was cooled to room temperature, quenched cautiously with aqueous Na2CO3, extracted with EtOAc (×2). The combined organic layer was washed with brine, dried over Na2SO4, and concentrated in vacuo. The residue was purified by chromatography on silica gel (0→30% EtOAc-hexanes) to yield the title compound.

후처리

  1. stirringThe mixture was stirred at room temperature for 2 h
  2. temperatureThe reaction was cooled to room temperature
  3. customquenched cautiously with aqueous Na2CO3
  4. extractionextracted with EtOAc (×2)
  5. washThe combined organic layer was washed with brine
  6. dry with materialdried over Na2SO4
  7. concentrationconcentrated in vacuo
  8. customThe residue was purified by chromatography on silica gel (0→30% EtOAc-hexanes)

출처 및 근거

ORD 기록
ord-4b2bfce924e244839466087a359646fb
출처 데이터셋
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08263767B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트