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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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N-[3-phenyl-3-(thien-2-yl)-2-propenyl]sarcosine ethyl ester → HCID 22225858, 화합물

HRID 635912
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반응식

HRID 635912 반응식
[CH2:1]([O:3][C:4](=[O:22])[CH2:5][N:6]([CH2:8][CH:9]=[C:10]([C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)[C:11]1[S:12][CH:13]=[CH:14][CH:15]=1)[CH3:7])[CH3:2]>CCO.[Pd]>[CH2:1]([O:3][C:4](=[O:22])[CH2:5][N:6]([CH2:8][CH2:9][CH:10]([C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)[C:11]1[S:12][CH:13]=[CH:14][CH:15]=1)[CH3:7])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 54147122N-[3-phenyl-3-(thien-2-yl)-2-propenyl]sarcosine ethyl ester2회

생성물 1

HCID 22225858HCID 22225858, 화합물수율 22%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

0.055 g (0.174 mmol) N-[3-Phenyl-3-(thien-2-yl)-2-propenyl]sarcosine ethyl ester (Compound 41 from Example 6) was hydrogenated over 0.055 g 10% Pd/C in 2 ml of EtOH. The hydrogenation was conducted at 40 psi for 16 hours at room temperature (see Reaction 20, FIG. 2). After filtering off the catalyst the solution was concentrated and the residue was purified by preparative TLC with 1:2 ethyl acetate:hexanes to give 0.012 g (22%) N-[3-phenyl-3-(thien-2-yl)propyl]sarcosine ethyl ester (Compound A42) as a yellow oil.

후처리

  1. custom(see Reaction 20, FIG. 2)
  2. filtrationAfter filtering off the catalyst the solution
  3. concentrationwas concentrated
  4. customthe residue was purified by preparative TLC with 1:2 ethyl acetate

출처 및 근거

ORD 기록
ord-6b607eb47f724f978b54f276485e80a2
출처 데이터셋
uspto-grants-2001_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06191165B1

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