Sodium Bicarbonate → HCID 68991018, 화합물

HRID 656970노트

반응식

HRID 656970 반응식
[ClH:1].Cl.[NH2:3][CH:4]1[CH2:9][CH2:8][N:7]([CH2:10][CH2:11][N:12]2[C:21]3[C:16](=[CH:17][CH:18]=[C:19]([F:22])[CH:20]=3)[N:15]=[CH:14][C:13]2=[O:23])[CH2:6][CH2:5]1.[O:24]1[C:28]2=[CH:29][N:30]=[C:31]([CH:33]=O)[CH:32]=[C:27]2[CH2:26][CH2:25]1.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].C(=O)(O)[O-].[Na+]>CO.C(Cl)(Cl)Cl.C(N(CC)CC)C>[ClH:1].[ClH:1].[O:24]1[C:28]2=[CH:29][N:30]=[C:31]([CH2:33][NH:3][CH:4]3[CH2:5][CH2:6][N:7]([CH2:10][CH2:11][N:12]4[C:21]5[C:16](=[CH:17][CH:18]=[C:19]([F:22])[CH:20]=5)[N:15]=[CH:14][C:13]4=[O:23])[CH2:8][CH2:9]3)[CH:32]=[C:27]2[CH2:26][CH2:25]1

참가 물질

8

실험 절차

A solution of 1-[2-(4-amino-1-piperidinyl)ethyl]-7-fluoro-2(1H)-quinoxalinone dihydrochloride (60 mg; 0.166 mmol) and 2,3-dihydrofuro[2,3-c]pyridine-5-carbaldehyde (30 mg, 0.20 mmol) in MeOH (3 ml), chloroform (3 ml) and triethylamine (0.06 ml) was heated under reflux with 3A molecular sieves overnight. It was cooled and sodium triacetoxyborohydride (0.11 g; 0.52 mmol) was added, and the mixture was stirred at rt overnight. Aqueous sodium bicarbonate solution was added to basify and the aqueous phase was extracted several times with 10% MeOH-DCM. The organic fractions were dried and evaporated. Chromatography on silica gel, eluting with 0-20% MeOH-DCM gave the free base of the title compound (50 mg, 71%).

후처리

  1. temperatureIt was cooled
  2. extractionthe aqueous phase was extracted several times with 10% MeOH-DCM
  3. customThe organic fractions were dried
  4. customevaporated
  5. washChromatography on silica gel, eluting with 0-20% MeOH-DCM

출처 및 근거

ORD 기록
ord-2e988a1cf247447ab030f16fcd78a85e
출처 데이터셋
uspto-grants-2011_12
특허 번호
US08071592B2

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