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

Diethyl Malonate → HCID 54692485, 화합물

HRID 601127
노트
인쇄 미리보기

반응식

HRID 601127 반응식
[H-].[Na+].[C:3]([O:11][CH2:12][CH3:13])(=[O:10])[CH2:4][C:5]([O:7]CC)=O.[CH2:14]([N:18]1[C:23]2[N:24]=[CH:25][CH:26]=[CH:27][C:22]=2C(=O)[O:20][C:19]1=O)[CH2:15][CH2:16][CH3:17]>CC(N(C)C)=O>[CH2:14]([N:18]1[C:23]2[C:22](=[CH:27][CH:26]=[CH:25][N:24]=2)[C:5]([OH:7])=[C:4]([C:3]([O:11][CH2:12][CH3:13])=[O:10])[C:19]1=[O:20])[CH2:15][CH2:16][CH3:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7761Diethyl MalonateHCID 24758Sodium hydrideHCID 103985421-butyl-2H-pyrido[2,3-d][1,3]oxazine-2,4(1H)-dione

생성물 1

HCID 54692485HCID 54692485, 화합물수율 70%

시약·촉매·용매 1

HCID 31374Dimethylacetamide용매

실험 절차

To a slurry of NaH (95%, 0.44 g, 18.2 mmol) in 15 mL anhydrous DMA at 10° C. under N2 was added diethyl malonate (2.9 g, 18.2 mmol) dropwise over 10 minutes. The mixture was stirred at ambient temperature for 30 minutes, treated with the product of Example 1B (2.0 g, 9.1 mmol) and heated at 120° C. for 3 hours. The mixture was cooled to ambient temperature and partitioned between ethyl acetate and cold water adjusting the pH to with 1 M HCl. The organic layer was washed 2×100 mL with water, 2×100 mL with saturated brine, dried (Na2SO4), filtered and the filtrate was concentrated under vacuum. The residue was recrystallized from hexane/ethyl acetate to give the desired compound as a white solid (1.84 g, 70% yield). MS (APCI+) m/z 291 (M+H)+.

후처리

  1. temperatureheated at 120° C. for 3 hours
  2. temperatureThe mixture was cooled to ambient temperature
  3. custompartitioned between ethyl acetate and cold water adjusting the pH to with 1 M HCl
  4. washThe organic layer was washed 2×100 mL with water, 2×100 mL with saturated brine
  5. dry with materialdried (Na2SO4)
  6. filtrationfiltered
  7. concentrationthe filtrate was concentrated under vacuum
  8. customThe residue was recrystallized from hexane/ethyl acetate

출처 및 근거

ORD 기록
ord-516084742d984785905c0256f78ed58c
출처 데이터셋
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07902203B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트