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Tetrahydrofuran → 6-(2,2-dimethylpropyl)-1,2,3,4-tetrahydro-2,2-dimethyl-4-Quinolinamine

HRID 20038
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HRID 20038 반응식
[CH2:1]([Mg]Cl)[C:2]([CH3:5])([CH3:4])[CH3:3].Br[C:9]1[CH:10]=[C:11]2[C:16](=[CH:17][CH:18]=1)[NH:15][C:14]([CH3:20])([CH3:19])[CH2:13][CH:12]2[NH2:21].O1CCCC1>[Cl-].[Zn+2].[Cl-]>[CH3:19][C:14]1([CH3:20])[CH2:13][CH:12]([NH2:21])[C:11]2[C:16](=[CH:17][CH:18]=[C:9]([CH2:1][C:2]([CH3:5])([CH3:4])[CH3:3])[CH:10]=2)[NH:15]1
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참가 물질

5

반응물 3

HCID 8028TetrahydrofuranHCID 673058276-bromo-1,2,3,4-tetrahydro-2,2-dimethyl-4-QuinolinamineHCID 178418809HCID 178418809, 화합물

생성물 1

HCID 673051226-(2,2-dimethylpropyl)-1,2,3,4-tetrahydro-2,2-dimethyl-4-Quinolinamine

시약·촉매·용매 1

HCID 3007855Zincchloride촉매

실험 절차

To neopentylmagnesium chloride (1.65 ml, 1.65 mmol) was added zinc(II) chloride (2.19 ml, 1.10 mmol) dropwise—strong exotherm was observed. The resulting mixture stirred for 10 minutes. A solution of 6-bromo-2,2-dimethyl-1,2,3,4-tetrahydroquinolin-4-amine (0.0700 g, 0.274 mmol) in tetrahydrofuran (1.37 ml, 0.274 mmol) was then added followed by palladium tetrakistriphenylphosphine (0.0317 g, 0.0274 mmol). The reaction vessel was sealed and heated to 65 deg C. The reaction mixture was stirred for 6 hours. The crude mixture was filtered through a plug of celite with EtOAc and concentrated in the presence of silica gel. The crude mixture was purified with the MPLC (100% DCM to 100% 90:10:1 DCM:MeOH:NH4OH) to provide the desired product. MS m/z: 230 (M−NH2).

후처리

  1. customThe reaction vessel was sealed
  2. temperatureheated to 65 deg C
  3. stirringThe reaction mixture was stirred for 6 hours
  4. filtrationThe crude mixture was filtered through a plug of celite with EtOAc
  5. concentrationconcentrated in the presence of silica gel
  6. customThe crude mixture was purified with the MPLC (100% DCM to 100% 90:10:1 DCM:MeOH:NH4OH)

출처 및 근거

ORD 기록
ord-858a129732b542ffb86522463a3809ce
출처 데이터셋
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07745484B2

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