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Ammonia → (1H-Benzoimidazol-5-yl)-(cis-2,3,4a,5,6,10b-hexahydro-1H-benzo[f]quinolin-4-yl)-methanone

HRID 2272030
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HRID 2272030 반응식
F[B-](F)(F)F.N1(OC(N(C)C)=[N+](C)C)C2C=CC=CC=2N=N1.F[P-](F)(F)(F)(F)F.N1(OC(N(C)C)=[N+](C)C)C2N=CC=CC=2N=N1.[NH:47]1[C:51]2[CH:52]=[CH:53][C:54]([C:56]([OH:58])=O)=[CH:55][C:50]=2[N:49]=[CH:48]1.C(N(C(C)C)C(C)C)C.[CH2:68]1[C@H:77]2[C@H:72]([CH2:73][CH2:74][C:75]3[CH:81]=[CH:80][CH:79]=[CH:78][C:76]=32)[NH:71][CH2:70][CH2:69]1.N>CN(C)C=O.CO.C(OCC)(=O)C>[NH:47]1[C:51]2[CH:52]=[CH:53][C:54]([C:56]([N:71]3[C@@H:72]4[C@@H:77]([C:76]5[CH:78]=[CH:79][CH:80]=[CH:81][C:75]=5[CH2:74][CH2:73]4)[CH2:68][CH2:69][CH2:70]3)=[O:58])=[CH:55][C:50]=2[N:49]=[CH:48]1
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참가 물질

10

반응물 6

HCID 222AmmoniaHCID 81531DiisopropylethylamineHCID 2733207O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 12327022(4aS,10bR)-1,2,3,4,4a,5,6,10b-Octahydrobenzo[f]quinoline
HCID 178524171
HCID 178524171, 화합물

생성물 1

HCID 178519358(1H-Benzoimidazol-5-yl)-(cis-2,3,4a,5,6,10b-hexahydro-1H-benzo[f]quinolin-4-yl)-methanone

시약·촉매·용매 3

HCID 887Methanol용매HCID 6228Dimethylformamide용매2회HCID 8857Ethyl Acetate용매

실험 절차

2-(1H-Benzotriazol-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate (0.50 g; alternatively, 2-(7-aza-1H-benzotriazol-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate may be used) is added to a solution of 1H-benzoimidazole-5-carboxylic acid (0.23 g) and ethyl-diisopropyl-amine (0.50 mL) in N,N-dimethylformamide (2 mL) at room temperature. The solution is stirred for 20 min prior to the addition of cis-1,2,3,4,4a,5,6,10b-octahydro-benzo[f]quinoline (0.30 g) dissolved in N,N-dimethylformamide (2 mL). The resulting solution is stirred at room temperature for 3 h. 32% aqueous ammonia (1 mL) in methanol (2 mL) is then added and the mixture is stirred for another 30 min. The mixture is diluted with ethyl acetate and washed with water and brine and dried (Na2SO4). The solvent is evaporated and the residue is chromatographed on silica gel (dichloromethane/methanol containing 1% NH3 95:5→80:20) to afford the title compound as a foam-like solid that is triturated with ether and dried to give a colorless solid [alternatively, the product may be purified by HPLC on reversed phase (MeOH/H2O)]. Yield: 0.38 g (80% of theory); LC (method 1): tR=2.53 min; Mass spectrum (ESI+): m/z=332 [M+H]+; 1H NMR (400 MHz, DMSO-d6, mixture of 2 rotamers) δ 1.52-1.82 (m, 4H), 1.82-1.94 (m, 1H), 2.24-ca. 2.48 (m, 1.5H), 2.71-3.02 (m, 3H), 3.03-3.18 (m, 0.5H), 3.50-3.65 (m, 0.5H), 3.88-4.05 (m, 0.5H), 4.39-4.56 (m, 0.5H), 4.83-4.99 (m, 0.5H), 6.89-7.20 (m, 4H), 7.21-7.27 (m, 1H), 7.56-7.70 (m, 2H), 8.23-8.35 (m, 1H), 12.58 (broad s, 1H).

후처리

  1. stirringThe resulting solution is stirred at room temperature for 3 h
  2. stirringthe mixture is stirred for another 30 min
  3. washwashed with water and brine
  4. dry with materialdried (Na2SO4)
  5. customThe solvent is evaporated
  6. customthe residue is chromatographed on silica gel (dichloromethane/methanol containing 1% NH3 95:5→80:20)

출처 및 근거

ORD 기록
ord-2c9ae66ad3e34f1e902ce5e38437fa00
출처 데이터셋
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09120769B2

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