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

Triethylamine → 2-(Azetidin-1-ylcarbonyl)-5-bromopyridine

HRID 600556
노트
인쇄 미리보기

반응식

HRID 600556 반응식
C(Cl)(=O)C(Cl)=O.[Br:7][C:8]1[CH:9]=[CH:10][C:11]([C:14]([OH:16])=O)=[N:12][CH:13]=1.O1CCOCC1.Cl.[NH:24]1[CH2:27][CH2:26][CH2:25]1.C(N(CC)CC)C>CN(C=O)C.Cl.C(Cl)Cl>[N:24]1([C:14]([C:11]2[CH:10]=[CH:9][C:8]([Br:7])=[CH:13][N:12]=2)=[O:16])[CH2:27][CH2:26][CH2:25]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

9

반응물 5

HCID 8471TriethylamineHCID 312751,4-DioxaneHCID 65578Oxalyl chlorideHCID 6085445-Bromopyridine-2-carboxylic acidHCID 12308726Azetidine hydrochloride

생성물 1

HCID 536296172-(Azetidin-1-ylcarbonyl)-5-bromopyridine수율 65%

시약·촉매·용매 3

HCID 6228
Dimethylformamide
촉매
HCID 313Hydrochloric Acid용매
HCID 6344Dichloromethane용매

실험 절차

Oxalyl chloride (11.5 mL, 130 mmol) then DMF (2 drops) were added to a mixture of 5-bromopyridine-2-carboxylic acid (CAS no. 30766-11-1) (12.6 g, 62.4 mmol) in 4M HCl in dioxane (15.6 mL, 74.9 mmol) and DCM (300 mL). The mixture was stirred at ambient temperature for 18 hours. The volatiles were removed under reduced pressure and azeotroped with toluene. The residue was dissolved in DCM (300 mL). Azetidine hydrochloride (6.14 g, 65.5 mmol) then triethylamine (24 mL, 187 mmol) were added and the mixture stirred at ambient temperature for 20 hours. The mixture was concentrated under reduced pressure and ethyl acetate (400 mL) added to the residue. The resulting mixture was washed with water (100 mL), filtered, washed with 1M citric acid solution (50 mL), saturated sodium bicarbonate solution (50 mL) and brine (50 mL), dried (MgSO4), filtered and the solvent removed under reduced pressure. The residue was purified by flash chromatography, eluting with a gradient of 0-40% ethyl acetate in isohexane to afford the product (8.8 g, 65%). m/z 242 (M+H)+.

후처리

  1. customThe volatiles were removed under reduced pressure
  2. customazeotroped with toluene
  3. dissolutionThe residue was dissolved in DCM (300 mL)
  4. stirringthe mixture stirred at ambient temperature for 20 hours
  5. concentrationThe mixture was concentrated under reduced pressure and ethyl acetate (400 mL)
  6. additionadded to the residue
  7. washThe resulting mixture was washed with water (100 mL)
  8. filtrationfiltered
  9. washwashed with 1M citric acid solution (50 mL), saturated sodium bicarbonate solution (50 mL) and brine (50 mL)
  10. dry with materialdried (MgSO4)
  11. filtrationfiltered
  12. customthe solvent removed under reduced pressure
  13. customThe residue was purified by flash chromatography
  14. washeluting with a gradient of 0-40% ethyl acetate in isohexane

출처 및 근거

ORD 기록
ord-4d0296ae03974dddbf18f0f5ed8fa0e9
출처 데이터셋
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07902200B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트