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Cesium carbonate → 4-(2-Methylsulfanyl-5,7-dihydro-pyrrolo[3,4-d]pyrimidin-6-yl)-pyridine-2-carboxylic acid (3-trifluoromethyl-phenyl)-amide

HRID 1052042
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HRID 1052042 반응식
Br[C:2]1[CH:7]=[CH:6][N:5]=[C:4]([C:8]([NH:10][C:11]2[CH:16]=[CH:15][CH:14]=[C:13]([C:17]([F:20])([F:19])[F:18])[CH:12]=2)=[O:9])[CH:3]=1.[CH3:21][S:22][C:23]1[N:24]=[CH:25][C:26]2[CH2:31][NH:30][CH2:29][C:27]=2[N:28]=1.C(=O)([O-])[O-].[Cs+].[Cs+].C1(P(C2C=CC=CC=2)C2C=CC3C(=CC=CC=3)C=2C2C3C(=CC=CC=3)C=CC=2P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>C([O-])(=O)C.[Pd+2].C([O-])(=O)C.C1(C)C=CC=CC=1>[F:18][C:17]([F:20])([F:19])[C:13]1[CH:12]=[C:11]([NH:10][C:8]([C:4]2[CH:3]=[C:2]([N:30]3[CH2:31][C:26]4[CH:25]=[N:24][C:23]([S:22][CH3:21])=[N:28][C:27]=4[CH2:29]3)[CH:7]=[CH:6][N:5]=2)=[O:9])[CH:16]=[CH:15][CH:14]=1
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참가 물질

7

반응물 4

HCID 10796Cesium carbonateHCID 634876Binap, (A+-)-HCID 670658482-(Methylthio)-6,7-dihydro-5H-pyrrolo[3,4-D]pyrimidineHCID 866958504-Bromo-N-(3-(trifluoromethyl)phenyl)picolinamide

생성물 1

HCID 866958544-(2-Methylsulfanyl-5,7-dihydro-pyrrolo[3,4-d]pyrimidin-6-yl)-pyridine-2-carboxylic acid (3-trifluoromethyl-phenyl)-amide수율 44.5%

시약·촉매·용매 2

HCID 167845palladium(II) acetate촉매HCID 1140Toluene용매

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온도
100 °C

실험 절차

To a toluene (5 mL) solution of 4-Bromo-N-(3-(trifluoromethyl)phenyl)picolinamide (172 mg, 0.50 mmol) and 2-(Methylthio)-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidine (84 mg, 0.50 mmol) was added cesium carbonate (325 mg, 1.00 mmol). The mixture was purged with nitrogen and then (±)-2,2′-bis(diphenylphosphino)-1,1′-binaphthalene (31 mg, 0.05 mmol) and palladium(II) acetate (11 mg, 0.05 mmol) were added. The reaction was capped and heated at 100° C. for 7 hours. The cooled mixture was filtered. The solid was rinsed twice with ethyl acetate then with chloroform:methanol (9:1). The combined filtrate was evaporated in vacuo. The solid was triturated with hexanes:ethyl acetate (1:1) followed by ethyl acetate:methanol (9:1) and gave the title compound (96 mg). The filtrate was chromatographed on silica gel (12 g) eluted with hexanes:ethyl acetate (1:1) and gave additional title compound (25 mg). The total amount of the title compound obtained was 120 mg (0.28 mmol, yield 56%).

후처리

  1. customThe mixture was purged with nitrogen
  2. customThe reaction was capped
  3. filtrationThe cooled mixture was filtered
  4. washThe solid was rinsed twice with ethyl acetate
  5. customThe combined filtrate was evaporated in vacuo
  6. customThe solid was triturated with hexanes:ethyl acetate (1:1)

출처 및 근거

ORD 기록
ord-560ae92663744dd193afbee952077e51
출처 데이터셋
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09388176B2

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