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

Methyl 4-Formylbenzoate → Methyl 4-[(R)-1-[(2S,5R)-4-Allyl-2,5-dimethyl-1-piperazinyl]-1-(3-tert-butyldimethylsilyloxyphenyl)methyl]benzoate

HRID 1057396
노트
인쇄 미리보기

반응식

HRID 1057396 반응식
[CH2:1]([N:4]1[CH2:9][C@H:8]([CH3:10])[NH:7][CH2:6][C@H:5]1[CH3:11])[CH:2]=[CH2:3].N1C2C=CC=CC=2N=N1.[CH:21]([C:23]1[CH:32]=[CH:31][C:26]([C:27]([O:29][CH3:30])=[O:28])=[CH:25][CH:24]=1)=O.[Si:33]([O:40][C:41]1[CH:42]=[C:43]([Mg]Br)[CH:44]=[CH:45][CH:46]=1)([C:36]([CH3:39])([CH3:38])[CH3:37])([CH3:35])[CH3:34]>C1(C)C=CC=CC=1.O1CCCC1.O>[CH2:1]([N:4]1[C@H:5]([CH3:11])[CH2:6][N:7]([C@H:21]([C:23]2[CH:32]=[CH:31][C:26]([C:27]([O:29][CH3:30])=[O:28])=[CH:25][CH:24]=2)[C:43]2[CH:44]=[CH:45][CH:46]=[C:41]([O:40][Si:33]([C:36]([CH3:39])([CH3:38])[CH3:37])([CH3:34])[CH3:35])[CH:42]=2)[C@@H:8]([CH3:10])[CH2:9]1)[CH:2]=[CH2:3]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 4

HCID 15294Methyl 4-FormylbenzoateHCID 10534891(-)-(2R,5S)-1-allyl-2,5-dimethylpiperazineHCID 178418385HCID 178418385, 화합물HCID 178455064HCID 178455064, 화합물

생성물 1

HCID 59037998Methyl 4-[(R)-1-[(2S,5R)-4-Allyl-2,5-dimethyl-1-piperazinyl]-1-(3-tert-butyldimethylsilyloxyphenyl)methyl]benzoate

시약·촉매·용매 3

HCID 962
Water
용매
HCID 1140Toluene용매
HCID 8028Tetrahydrofuran용매

반응 조건

온도
-17.5 °C

실험 절차

A solution of (−)-(2R,5S)-1-allyl-2,5-dimethylpiperazine (22.26 g), benzotriazole (17.18 g) and methyl 4-formylbenzoate (23.7 g) in toluene (400 ml) was heated under reflux with azeotropic removal of water for 3 hours. The solution was cooled and added to a cold solution (−20° C.) of 3-tert-butyldimethylsilyloxyphenylmagnesium bromide (prepared from 82.9 g of corresponding bromide and 7.29 g of magnesium turnings) in tetrahydrofuran (300 ml) at such a rate as to maintain the internal temperature in the range −20 to −15° C. The resulting solution was stirred at −20° C. for 1.5 hours and then warmed to room temperature, quenched with saturated aqueous ammonium chloride solution (200 ml). The layers were separated and the aqueous solution extracted with ethyl acetate (2×200 ml). The combined organic extracts were dried (MgSO4) and evaporated to dryness in vacuo. The residue was purified by column chromatography over silica gel (85/15/2 hexane/ethyl acetate/diethyl amine) to afford the title compound, 54.45 g.

후처리

  1. temperatureThe solution was cooled
  2. temperaturewarmed to room temperature
  3. customquenched with saturated aqueous ammonium chloride solution (200 ml)
  4. customThe layers were separated
  5. extractionthe aqueous solution extracted with ethyl acetate (2×200 ml)
  6. dry with materialThe combined organic extracts were dried (MgSO4)
  7. customevaporated to dryness in vacuo
  8. customThe residue was purified by column chromatography over silica gel (85/15/2 hexane/ethyl acetate/diethyl amine)

출처 및 근거

ORD 기록
ord-ebd0c3692d3646278f632ab9c539bd39
출처 데이터셋
uspto-grants-2003_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06514975B1

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트