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Cesium carbonate → HCID 117643277, 화합물

HRID 2171280
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HRID 2171280 반응식
[NH2:1][C:2]1(C)[CH:7]=C[CH:5]=[N:4][CH2:3]1.[C:9](=[O:12])([O-])[O-:10].[Cs+].[Cs+].C[C:16]1(C)[C:42]2[C:37](=[C:38](P(C3C=CC=CC=3)C3C=CC=CC=3)[CH:39]=[CH:40][CH:41]=2)OC2C(P(C3C=CC=CC=3)C3C=CC=CC=3)=CC=CC1=2.Cl[C:58]1[N:63]=[C:62]([NH:64][CH:65]2[CH2:70][CH2:69][N:68](C(OCC3C=CC=CC=3)=O)[CH2:67][CH:66]2[N:81]2[C:89](=[O:90])[C:88]3[C:83](=[CH:84][CH:85]=[CH:86][CH:87]=3)[C:82]2=[O:91])[C:61]([F:92])=[CH:60][C:59]=1[C:93]#[N:94].O1[CH2:100][CH2:99]OCC1>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]>[C:93]([C:59]1[CH:60]=[C:61]([F:92])[C:62]([NH:64][CH:65]2[CH2:70][CH2:69][N:68]([C:9]([O:10][CH2:16][C:42]3[CH:37]=[CH:38][CH:39]=[CH:40][CH:41]=3)=[O:12])[CH2:67][CH:66]2[N:81]2[C:82](=[O:91])[C:83]3[C:88](=[CH:87][CH:86]=[CH:85][CH:84]=3)[C:89]2=[O:90])=[N:63][C:58]=1[NH:1][C:2]1[CH:3]=[N:4][CH:5]=[C:99]([CH3:100])[CH:7]=1)#[N:94]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 5

HCID 10796Cesium carbonateHCID 312751,4-DioxaneHCID 6360441,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 89174215HCID 89174215, 화합물HCID 117643958HCID 117643958, 화합물

생성물 1

HCID 117643277HCID 117643277, 화합물

시약·촉매·용매

1
HCID 9811564Bis(dibenzylideneacetone)palladium촉매

실험 절차

3-Amino-3-methylpyridine (9 mg), cesium carbonate (45 mg), Pd2(dba)3 (10 mg), and Xantphos (12 mg) were added to a dioxane (3 ml) solution containing benzyl 4-((6-chloro-5-cyano-3-fluoropyridin-2-yl)amino)-3-(1,3-dioxoisoindolin-2-yl)piperidin-1-carboxylate (37 mg), followed by microwave irradiation (Initiator™, 160° C., 10 minutes, 2.45 GHz, 0-240 W). The obtained residue was filtered through Celite and filter cake was washed with ethyl acetate. Subsequently, the solvent was distilled away from the filtrate under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate=4:1 to 1:1). Yellow oily matter of benzyl 4-((5-cyano-3-fluoro-6-((5-methylpyridin-3-yl)amino)pyridin-2-yl)amino)-3-(1,3-dioxoisoindolin-2-yl)piperidin-1-carboxylate (28 mg) was thus obtained.

후처리

  1. customfollowed by microwave irradiation (Initiator™, 160° C., 10 minutes, 2.45 GHz, 0-240 W)
  2. filtrationThe obtained residue was filtered through Celite
  3. filtrationfilter cake
  4. washwas washed with ethyl acetate
  5. distillationSubsequently, the solvent was distilled away from the filtrate under reduced pressure
  6. customThe obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate=4:1 to 1:1)

출처 및 근거

ORD 기록
ord-4492ee030fb946bfaf76680e36f1553c
출처 데이터셋
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09051310B2

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