Iodine → HCID 57831240, 화합물

HRID 453894노트

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HRID 453894 반응식
II.[Mg].Br[C:5]1[S:6][CH:7]=[CH:8][CH:9]=1.[C:10]([O:14][C:15]([N:17]1[CH2:22][CH2:21][C:20](C#N)([N:23]([CH3:25])[CH3:24])[CH2:19][CH2:18]1)=[O:16])([CH3:13])([CH3:12])[CH3:11].[NH4+].[Cl-]>C(OCC)C.C1COCC1>[C:10]([O:14][C:15]([N:17]1[CH2:18][CH2:19][C:20]([N:23]([CH3:25])[CH3:24])([C:5]2[S:6][CH:7]=[CH:8][CH:9]=2)[CH2:21][CH2:22]1)=[O:16])([CH3:13])([CH3:12])[CH3:11]

참가 물질

8

반응물 5

HCID 807IodineHCID 138512-Bromothiophene2회HCID 25517Ammonium ChlorideHCID 5462224MagnesiumHCID 57504797Tert-butyl 4-cyano-4-(dimethylamino)piperidine-1-carboxylate

생성물 1

HCID 57831240HCID 57831240, 화합물수율 64.1%

시약·촉매·용매 2

HCID 3283Diethyl Ether용매2회HCID 8028Tetrahydrofuran용매

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온도
0 °C

실험 절차

A little iodine was added to a mixture of 5.6 g (3 eq.) magnesium and 20 ml dry diethyl ether, followed over a period of 10 min by 5 g 2-bromothiophene, and the mixture was stirred for a further 10 min. Once the reaction had started, 33.5 g (2.6 eq.) 2-bromothiophene dissolved in 80 ml diethyl ether were added dropwise and the mixture was stirred for a period of 2 h at room temperature. The Grignard reagent prepared in the preceding step was added dropwise to a solution of 20 g (1 eq.) tert-butyloxycarbonyl-4-cyano-4-(dimethylamino)piperidine dissolved in 200 ml THF and stirred overnight at room temperature. Once the conversion was complete, the reaction solution was cooled to 0° C., mixed with saturated NH4Cl solution, extracted with ethyl acetate (3×100 ml) and the combined organic phases were dried with Na2SO4. Following removal of the solvent under reduced pressure, the residue was purified by column chromatography (alox neutral; 30% EtOAc/hexane). 6.1 g (25%) of product were obtained in the form of a white solid.

후처리

  1. additionwere added dropwise
  2. stirringthe mixture was stirred for a period of 2 h at room temperature
  3. stirringstirred overnight at room temperature
  4. extractionextracted with ethyl acetate (3×100 ml)
  5. dry with materialthe combined organic phases were dried with Na2SO4
  6. customremoval of the solvent under reduced pressure
  7. customthe residue was purified by column chromatography (alox neutral; 30% EtOAc/hexane)

출처 및 근거

ORD 기록
ord-ce605e55236c456488cfea70f48c0155
출처 데이터셋
uspto-grants-2013_07
특허 번호
US08492559B2

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