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Methanol → Lupinane

HRID 2175387
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HRID 2175387 반응식
[C@H:1]1([CH2:11]N)[C@@H:10]2[N:5]([CH2:6][CH2:7][CH2:8][CH2:9]2)[CH2:4][CH2:3][CH2:2]1.C([O-])(O)=O.[Na+].CO>O>[CH3:11][C@H:1]1[C@H:10]2[CH2:9][CH2:8][CH2:7][CH2:6][N:5]2[CH2:4][CH2:3][CH2:2]1
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참가 물질

5

반응물 3

HCID 887MethanolHCID 516892Sodium BicarbonateHCID 6358779HCID 6358779, 화합물

생성물 1

HCID 60028369Lupinane

시약·촉매·용매 1

HCID 962Water용매

실험 절차

The lupinane amine.2HCl (1-[(1S,9aR)-octahydro-2H-quinolizin-1-yl]methanamine, CAS #: 75532-84-2, commercially available from ChemBridge, San Diego) (1.0 eq) was combined with 2,4-dichloro-5-X-pyrimidine (X=H, F, Cl, Me, CF3, CN, CONH2, OMe, NMe2) (1.0 eq) and NaHCO3 (1.2 eq). A mixture of MeOH:H2O (4/1) (concentration of the reaction mixture: ca. 0.1-0.5 M) was added and the resulting suspension was stirred for 1 d at RT. After the completion of the reaction was confirmed by TLC and HPLC, silica gel was added to the reaction mixture and solvents were evaporated under reduced pressure. The resulting solid was loaded on a CombiFlash column and further purified by flash chromatography eluting with DCM/MeOH—NH3 (2M) (gradient 0->10%).

후처리

  1. additionwas added to the reaction mixture and solvents
  2. customwere evaporated under reduced pressure
  3. customfurther purified by flash chromatography
  4. washeluting with DCM/MeOH—NH3 (2M) (gradient 0->10%)

출처 및 근거

ORD 기록
ord-c6e7ef7d835a4128a115247530da3b20
출처 데이터셋
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09062068B2

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