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

Ethyl 2-(4,6-dimethyl-5-nitropyrimidine-2-yloxy)acetate → Ethyl 2-(5-amino-4,6-dimethylpyrimidine-2-yloxy)acetate

HRID 2280889
노트
인쇄 미리보기

반응식

HRID 2280889 반응식
[CH3:1][C:2]1[C:7]([N+:8]([O-])=O)=[C:6]([CH3:11])[N:5]=[C:4]([O:12][CH2:13][C:14]([O:16][CH2:17][CH3:18])=[O:15])[N:3]=1.[H][H]>C(O)C.[Pd]>[NH2:8][C:7]1[C:2]([CH3:1])=[N:3][C:4]([O:12][CH2:13][C:14]([O:16][CH2:17][CH3:18])=[O:15])=[N:5][C:6]=1[CH3:11]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 59336196Ethyl 2-(4,6-dimethyl-5-nitropyrimidine-2-yloxy)acetateHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 59336106Ethyl 2-(5-amino-4,6-dimethylpyrimidine-2-yloxy)acetate수율 99.9%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

반응 조건

온도
25 °C

실험 절차

Compound 6 (75.98 g) and 5% Pd—C (7.598 g, N. E. CHEMCAT, STD Type) were suspended in ethanol (760 mL). Evacuation and replacement with hydrogen were repeated three times. Subsequently, the suspension was vigorously stirred at room temperature (20 to 30° C.) for 4.5 hours under hydrogen atmosphere. After the reaction was completed, the mixture was subjected to high precision pressure filtration (0.2 μm, PTFE) and the filtered product was washed with ethanol (474 mL). The filtrate was evaporated under reduced pressure to give 66.99 g (99.9% yield) of the desired product as a pale yellow solid.

후처리

  1. filtrationthe mixture was subjected to high precision pressure filtration (0.2 μm, PTFE)
  2. washthe filtered product was washed with ethanol (474 mL)
  3. customThe filtrate was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-360173c0d7e94654a80bd4f0de06a275
출처 데이터셋
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09139559B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트