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

Lithium Hydroxide → (S)-3-(4-(3,4-Bis(trifluoromethoxy)benzyloxy)phenyl)-3-(isoxazol-3-yl)propanoic acid

HRID 2235591
노트
인쇄 미리보기

반응식

HRID 2235591 반응식
[C:1](=[O:4])([O-])[O-:2].[Cs+].[Cs+].Br[CH2:8][C:9]1[CH:14]=[CH:13][C:12]([O:15][C:16]([F:19])([F:18])[F:17])=[C:11]([O:20][C:21]([F:24])([F:23])[F:22])[CH:10]=1.C([C@H]1COC(=O)N1C(=O)[CH2:39][C@@H:40]([C:46]1[CH:51]=[CH:50][C:49]([OH:52])=[CH:48][CH:47]=1)[C:41]1[CH:45]=[CH:44][O:43][N:42]=1)C1C=CC=CC=1.[Li+].[OH-]>CN(C=O)C.O.C1COCC1>[F:22][C:21]([F:24])([F:23])[O:20][C:11]1[CH:10]=[C:9]([CH:14]=[CH:13][C:12]=1[O:15][C:16]([F:19])([F:18])[F:17])[CH2:8][O:52][C:49]1[CH:48]=[CH:47][C:46]([C@@H:40]([C:41]2[CH:45]=[CH:44][O:43][N:42]=2)[CH2:39][C:1]([OH:2])=[O:4])=[CH:51][CH:50]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 4

HCID 3939Lithium HydroxideHCID 10796Cesium carbonateHCID 451566974-(Bromomethyl)-1,2-bis(trifluoromethoxy)benzeneHCID 57801829(S)-4-Benzyl-3-((S)-3-(4-hydroxyphenyl)-3-(isoxazol-3-yl)propanoyl)oxazolidin-2-one

생성물 1

HCID 24898112(S)-3-(4-(3,4-Bis(trifluoromethoxy)benzyloxy)phenyl)-3-(isoxazol-3-yl)propanoic acid수율 18.4%

시약·촉매·용매 3

HCID 962Water용매HCID 6228Dimethylformamide용매HCID 8028Tetrahydrofuran용매

실험 절차

Cesium carbonate (137 mg, 0.4 mmol) was added to a mixture of 4-(bromomethyl)-1,2-bis(trifluoromethoxy)benzene 22.1 (71 mg, 0.21 mmol) and 7.5 (82 mg, 0.21 mmol) in DMF (2 mL). The mixture was stirred at room temperature for 16 hours. To the reaction mixture was added LiOH in water (0.5 mL, 1N solution) and THF (1 mL). The mixture was stirred at 23° C. for 3 hours. The mixture was filtered and purified by reverse phase HPLC to give 22 (19 mg) after lyophilization. MS ESI (pos.) m/e 492.1 (M+H). 1H NMR (400 MHz, CDCl3) δ 8.31 (1H, s), 7.45 (1H, s), 7.39 (2H, s), 7.21 (2H, d, J=8.3 Hz), 6.93 (2H, d, J=8.8 Hz), 6.08 (1H, s), 5.05 (2H, s), 4.57 (1H, t, J=7.6 Hz), 3.37 (1H, dd, J=16.6, 7.8 Hz), 3.00 (1H, dd, J=16.6, 7.8 Hz).

후처리

  1. stirringThe mixture was stirred at 23° C. for 3 hours
  2. filtrationThe mixture was filtered
  3. custompurified by reverse phase HPLC

출처 및 근거

ORD 기록
ord-48dd3a8948d44d5d8fbd5b53ce384cbb
출처 데이터셋
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07714008B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트