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tert-butyl (3R)-3-aminopiperidine-1-carboxylate → (R)-tert-butyl 3-((1-methyl-1H-pyrrolo[2,3-c]pyridin-7-yl)amino)piperidine-1-carboxylate

HRID 588360
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HRID 588360 반응식
CC(C1C=C(C(C)C)C(C2C(P(C3CCCCC3)C3CCCCC3)=C(OC)C=CC=2OC)=C(C(C)C)C=1)C.CC([O-])(C)C.[Na+].Cl[C:46]1[N:47]=[CH:48][CH:49]=[C:50]2[CH:54]=[CH:53][N:52]([CH3:55])[C:51]=12.[NH2:56][C@@H:57]1[CH2:62][CH2:61][CH2:60][N:59]([C:63]([O:65][C:66]([CH3:69])([CH3:68])[CH3:67])=[O:64])[CH2:58]1>C1(C)C=CC=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].[Pd].O>[CH3:55][N:52]1[C:51]2=[C:46]([NH:56][C@@H:57]3[CH2:62][CH2:61][CH2:60][N:59]([C:63]([O:65][C:66]([CH3:69])([CH3:68])[CH3:67])=[O:64])[CH2:58]3)[N:47]=[CH:48][CH:49]=[C:50]2[CH:54]=[CH:53]1
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참가 물질

8

반응물 4

HCID 1501974tert-butyl (3R)-3-aminopiperidine-1-carboxylateHCID 23676156Sodium t-butoxideHCID 25112535BrettphosHCID 594244767-chloro-1-methyl-1H-pyrrolo[2,3-c]pyridine2회

생성물 1

HCID 117652959(R)-tert-butyl 3-((1-methyl-1H-pyrrolo[2,3-c]pyridin-7-yl)amino)piperidine-1-carboxylate수율 94%

시약·촉매·용매 3

HCID 9811564Bis(dibenzylideneacetone)palladium촉매HCID 962Water용매HCID 1140Toluene용매

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온도
105 °C

실험 절차

A solution of Pd2(dba)3 (1.53 g, 1.68 mmol), BrettPhos (1.86 g, 3.36 mmol) in toluene (40 mL) under N2 atmosphere was stirred for 20 min. NaOtBu (3.23 g, 33.6 mmol), the compound from Step 1 7-chloro-1-methyl-1H-pyrrolo[2,3-c]pyridine (2.80 g, 16.8 mmmol) and tert-butyl (3R)-3-aminopiperidine-1-carboxylate (4.04 g, 20.2 mmol) were added. The reaction was stirred at 105° C. for 3 h. The reaction mixture was poured into water (20 mL) and extracted with EtOAc (3×20 mL). The organic layers were dried over Na2SO4, filtered and the filtrate was concentrated in vacuo. The residue was purified by silica gel column chromatography, eluting with a gradient of 17-50% EtOAc/petroleum ether to give the title compound as a brown solid (5.2 g, 94%).

후처리

  1. extractionextracted with EtOAc (3×20 mL)
  2. dry with materialThe organic layers were dried over Na2SO4
  3. filtrationfiltered
  4. concentrationthe filtrate was concentrated in vacuo
  5. customThe residue was purified by silica gel column chromatography
  6. washeluting with a gradient of 17-50% EtOAc/petroleum ether

출처 및 근거

ORD 기록
ord-c656875441234c8a95f0cc918694e41d
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09227956B2

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