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Tetrahydrofuran → HCID 44160016, 화합물

HRID 1926304
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HRID 1926304 반응식
[NH2:1][C:2]1[N:7]=[CH:6][C:5]([C:8]2[CH:9]=[N:10][N:11]([CH:13]3[CH2:18][CH2:17][N:16]([CH:19]=O)[CH2:15][CH2:14]3)[CH:12]=2)=[CH:4][C:3]=1[C:21]1[N:22]=[CH:23][C:24]2[C:29]([CH:30]=1)=[C:28]([Cl:31])[CH:27]=[CH:26][C:25]=2[F:32].C1COCC1.[H-].[H-].[H-].[H-].[Li+].[Al+3].O.O.O.O.O.O.O.O.O.O.S([O-])([O-])(=O)=O.[Na+].[Na+]>CCOC(C)=O>[Cl:31][C:28]1[CH:27]=[CH:26][C:25]([F:32])=[C:24]2[C:29]=1[CH:30]=[C:21]([C:3]1[C:2]([NH2:1])=[N:7][CH:6]=[C:5]([C:8]3[CH:9]=[N:10][N:11]([CH:13]4[CH2:14][CH2:15][N:16]([CH3:19])[CH2:17][CH2:18]4)[CH:12]=3)[CH:4]=1)[N:22]=[CH:23]2
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 8028TetrahydrofuranHCID 62649Sodium sulfate decahydrateHCID 21226445Aluminium lithium hydrideHCID 866331564-{4-[6-Amino-5-(5-chloro-8-fluoroisoquinolin-3-yl)-pyridin-3-yl]-pyrazol-1-yl}-piperidine-1-carbaldehyde

생성물 1

HCID 44160016HCID 44160016, 화합물

시약·촉매·용매 1

HCID 8857
Ethyl Acetate
용매

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온도
0 °C

실험 절차

To a solution of 4-{4-[6-amino-5-(5-chloro-8-fluoroisoquinolin-3-yl)-pyridin-3-yl]-pyrazol-1-yl}-piperidine-1-carbaldehyde (50.0 mg, 0.111 mmol) in THF (5 mL, 60 mmol), cooled to ≈0° C., LiAlH4 (1.0M solution in THF; 0.27 mL, 0.27 mmol) was added, and the reaction mixture was stirred at 0° C.→rt for 30 min. Sodium sulfate decahydrate (0.1 g, 0.4 mmol) and EtOAc were added and the reaction mixture was stirred for 10 min at rt. The solids were filtered off, and the filtrate was concentrated and purified on prep-TLC eluting with 5% 7M NH3 (MeOH)/DCM to give the title compound as pale yellow oil. MS (ES+): m/z=436.79/438.74 [MH+]. HPLC: tR=2.24 min (ZQ2, polar—5 min).

후처리

  1. stirringthe reaction mixture was stirred for 10 min at rt
  2. filtrationThe solids were filtered off
  3. concentrationthe filtrate was concentrated
  4. custompurified
  5. washon prep-TLC eluting with 5% 7M NH3 (MeOH)/DCM

출처 및 근거

ORD 기록
ord-7127344ba85744ccbc2bd3f23052e9e6
출처 데이터셋
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08178668B2

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