Diisopropylethylamine → [2-(2,5-Dichloro-phenoxy)-pyridin-3-yl]-(2,3,3a,4-tetrahydro-1H-pyrrolo[1,2-a]quinoxalin-5-yl)-methanone

HRID 1877398노트

반응식

HRID 1877398 반응식
[CH:1]1[N:5]2[C:6]3[C:11]([NH:12][CH2:13][C:4]2=[CH:3][CH:2]=1)=[CH:10][CH:9]=[CH:8][CH:7]=3.C(N(C(C)C)C(C)C)C.[Cl:23][C:24]1[CH:48]=[CH:47][C:46]([Cl:49])=[CH:45][C:25]=1[O:26][C:27]1[C:32]([C:33](N2C3C(=CC=CC=3)NCC2)=[O:34])=[CH:31][CH:30]=[CH:29][N:28]=1>C(O)C.[Pd]>[Cl:23][C:24]1[CH:48]=[CH:47][C:46]([Cl:49])=[CH:45][C:25]=1[O:26][C:27]1[C:32]([C:33]([N:12]2[C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[N:5]3[CH2:1][CH2:2][CH2:3][CH:4]3[CH2:13]2)=[O:34])=[CH:31][CH:30]=[CH:29][N:28]=1

참가 물질

6

반응물 3

HCID 81531DiisopropylethylamineHCID 118051814,5-Dihydropyrrolo[1,2-a]quinoxalineHCID 59294486[2-(2,5-Dichloro-phenoxy)-pyridin-3-yl]-(3,4-dihydro-2H-quinoxalin-1-yl)-methanone

생성물 1

HCID 59294531[2-(2,5-Dichloro-phenoxy)-pyridin-3-yl]-(2,3,3a,4-tetrahydro-1H-pyrrolo[1,2-a]quinoxalin-5-yl)-methanone수율 32.4%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

To a solution of 4,5-dihydro-pyrrolo[1,2-α]quinoxaline (30.6 mg, 0.18 mmol, 1.2 equiv; [CAS RN 56721-86-9]) in ethanol (5 mL) was added palladium on carbon (3.2 mg, 0.003 mmol, 0.02 equiv; 10% Pd/C; [CAS RN 7440-05-3]) and the reaction mixture stirred under an atmosphere of hydrogen (3 bar) at rt for 4 h. The reaction mixture was concentrated under reduced pressure, filtered over Celite® and the remaining residue redissolved in anhydrous DMF (1 mL). To this solution was added N-ethyldiisopropylamine (64 mg, 86 μL, 0.50 mmol, 5.0 equiv; [CAS RN 7087-68-5]) and 2-(2,5-dichloro-phenoxy)-nicotinoylchloride (45.4 mg, 0.15 mmol, 1.0 equiv; prepared according to Example 122) and the reaction mixture stirred at rt over night. Removal of the solvent mixture under reduced pressure and purification by preparative HPLC on reversed phase (Xterra® PrepMSC 18, 5 μm, 19×50 mm column equipped with a Gilson Liquid Handler 215 autosampler, two Rainin Dynamax® SD-300 pumps, a Sedex ELSD 75 lightscatter and a Dionex UVD 340S UV detector) eluting with a gradient of acetonitrile/water provided 21.4 mg (32%) of the title compound. MS (ISP): 440.1 [M+H]+.

후처리

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. filtrationfiltered over Celite®
  3. dissolutionthe remaining residue redissolved in anhydrous DMF (1 mL)
  4. stirringthe reaction mixture stirred at rt over night
  5. customRemoval of the solvent mixture
  6. customunder reduced pressure and purification by preparative HPLC on reversed phase (Xterra® PrepMSC 18, 5 μm, 19×50 mm column
  7. customequipped with a Gilson Liquid Handler 215 autosampler, two Rainin Dynamax® SD-300 pumps
  8. washa Sedex ELSD 75 lightscatter and a Dionex UVD 340S UV detector) eluting with a gradient of acetonitrile/water

출처 및 근거

ORD 기록
ord-9219f11e0d454314afdad1913c4bf57b
출처 데이터셋
uspto-grants-2012_11
특허 번호
US08309734B2

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