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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Diiodomethane → (3R,9S)-9-(tert-butyldimethylsilyloxy)-7,7-dimethyl-4-(1-methylcyclopropyl)-3-(4-(trifluoromethyl)phenyl)-2',3',5',6,6',7,8,9-octahydro-3H-spiro[furo[3,4-c]quinoline-1,4'-pyran]

HRID 573786
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HRID 573786 반응식
[CH2:1]([Zn]CC)C.FC(F)(F)C(O)=O.ICI.[Si:16]([O:23][C@H:24]1[CH2:33][C:32]([CH3:35])([CH3:34])[CH2:31][C:30]2[N:29]=[C:28]([C:36]([CH3:38])=[CH2:37])[C:27]3[C@@H:39]([C:47]4[CH:52]=[CH:51][C:50]([C:53]([F:56])([F:55])[F:54])=[CH:49][CH:48]=4)[O:40][C:41]4([CH2:46][CH2:45][O:44][CH2:43][CH2:42]4)[C:26]=3[C:25]1=2)([C:19]([CH3:22])([CH3:21])[CH3:20])([CH3:18])[CH3:17]>ClCCl>[Si:16]([O:23][C@H:24]1[CH2:33][C:32]([CH3:35])([CH3:34])[CH2:31][C:30]2[N:29]=[C:28]([C:36]3([CH3:1])[CH2:38][CH2:37]3)[C:27]3[C@@H:39]([C:47]4[CH:52]=[CH:51][C:50]([C:53]([F:56])([F:54])[F:55])=[CH:49][CH:48]=4)[O:40][C:41]4([CH2:46][CH2:45][O:44][CH2:43][CH2:42]4)[C:26]=3[C:25]1=2)([C:19]([CH3:20])([CH3:21])[CH3:22])([CH3:18])[CH3:17]
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HCID 6346DiiodomethaneHCID 6422Trifluoroacetic acidHCID 66762113(3R,9S)-9-(tert-butyldimethylsilyloxy)-7,7-dimethyl-4-(prop-1-en-2-yl)-3-(4-(trifluoromethyl)phenyl)-2',3',5',6,6',7,8,9-octahydro-3H-spiro[furo[3,4-c]quinoline-1,4'-pyran]HCID 178418750HCID 178418750, 화합물

생성물 1

HCID 66761645
(3R,9S)-9-(tert-butyldimethylsilyloxy)-7,7-dimethyl-4-(1-methylcyclopropyl)-3-(4-(trifluoromethyl)phenyl)-2',3',5',6,6',7,8,9-octahydro-3H-spiro[furo[3,4-c]quinoline-1,4'-pyran]

시약·촉매·용매 1

HCID 6344Dichloromethane용매4회

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온도
0 °C

실험 절차

536 μl Diethylzinc (1 M in n-hexane) are dissolved in 5 ml dichloromethane, cooled to 0° C. and treated dropwise with a solution of 41 μl trifluoroacetic acid in 5 ml dichloromethane. The mixture is stirred for 20 minutes and then 41 μl diiodomethane in 2.5 ml dichloromethane are added dropwise. After stirring for further 20 minutes a solution of 150 mg (3R,9S)-9-(tert-butyldimethylsilyloxy)-7,7-dimethyl-4-(prop-1-en-2-yl)-3-(4-(trifluoromethyl)phenyl)-2′,3′,5′,6,6′,7,8,9-octahydro-3H-spiro[furo[3,4-c]quinoline-1,4′-pyran] in 2.5 ml dichloromethane are added dropwise. The mixture is then allowed to warm to room temperature and is stirred for 4 hours. Then it is partitioned between saturated solution of sodium bicarbonate in water and dichloromethane. The aqueous phase is twice extracted with dichloromethane. The combined organic phases are dried with sodium sulphate and the solvents are evaporated in vacuo. The residue is chromatographed on silica gel (petrole ether/ethylacetate 100:0 to 85:15).

후처리

  1. additionare added dropwise
  2. temperatureto warm to room temperature
  3. stirringis stirred for 4 hours
  4. customThen it is partitioned between saturated solution of sodium bicarbonate in water and dichloromethane
  5. extractionThe aqueous phase is twice extracted with dichloromethane
  6. dry with materialThe combined organic phases are dried with sodium sulphate
  7. customthe solvents are evaporated in vacuo
  8. customThe residue is chromatographed on silica gel (petrole ether/ethylacetate 100:0 to 85:15)

출처 및 근거

ORD 기록
ord-8bfa8cfc1fc74ff58ee0f8e392218a25
출처 데이터셋
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09029544B2

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