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Toluene → Tert-butyl (2-chloro-5-(difluoromethyl)-3-(4-(oxetan-3-yl)piperazin-1-yl)phenyl)(4-methoxybenzyl)carbamate

HRID 921664
ノート
印刷プレビュー

反応式

HRID 921664 の反応式
C(=O)([O-])[O-].[Cs+].[Cs+].C1C=CC(P(C2C(C3C(P(C4C=CC=CC=4)C4C=CC=CC=4)=CC=C4C=3C=CC=C4)=C3C(C=CC=C3)=CC=2)C2C=CC=CC=2)=CC=1.[O:53]1[CH2:56][CH:55]([N:57]2[CH2:62][CH2:61][NH:60][CH2:59][CH2:58]2)[CH2:54]1.Br[C:64]1[C:65]([Cl:90])=[C:66]([N:73]([CH2:81][C:82]2[CH:87]=[CH:86][C:85]([O:88][CH3:89])=[CH:84][CH:83]=2)[C:74](=[O:80])[O:75][C:76]([CH3:79])([CH3:78])[CH3:77])[CH:67]=[C:68]([CH:70]([F:72])[F:71])[CH:69]=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]>[Cl:90][C:65]1[C:64]([N:60]2[CH2:61][CH2:62][N:57]([CH:55]3[CH2:56][O:53][CH2:54]3)[CH2:58][CH2:59]2)=[CH:69][C:68]([CH:70]([F:72])[F:71])=[CH:67][C:66]=1[N:73]([CH2:81][C:82]1[CH:83]=[CH:84][C:85]([O:88][CH3:89])=[CH:86][CH:87]=1)[C:74](=[O:80])[O:75][C:76]([CH3:79])([CH3:78])[CH3:77]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 1140TolueneHCID 10796Cesium carbonateHCID 634876Binap, (A+-)-HCID 574162871-(Oxetan-3-yl)piperazineHCID 86708468Tert-butyl (3-bromo-2-chloro-5-(difluoromethyl)phenyl)(4-methoxybenzyl)carbamate

生成物 1

HCID 86708530
Tert-butyl (2-chloro-5-(difluoromethyl)-3-(4-(oxetan-3-yl)piperazin-1-yl)phenyl)(4-methoxybenzyl)carbamate

試薬・触媒・溶媒 1

HCID 9811564Bis(dibenzylideneacetone)palladium触媒

反応条件

温度
106 °C

実験手順

Cesium carbonate (672 mg, 2.063 mmol), BINAP (64.2 mg, 0.103 mmol), 1-(oxetan-3-yl)piperazine (176 mg, 1.238 mmol) and Pd2(dba)3 (94 mg, 0.103 mmol) were weighed into a 25 mL round bottom flask at room temperature. A solution of tert-butyl (3-bromo-2-chloro-5-(difluoromethyl)phenyl)(4-methoxybenzyl)carbamate in toluene (4294 μl, 1.031 mmol) was added and the reaction was degassed 3 times by evacuating the flask under vacuum and then purging with N2. The reaction mixture was heated to 106° C. for 16 h and then cooled to room temperature. The reaction mixture was diluted with EtOAc, sonicated, filtered through celite and concentrated. The product was purified by column chromatography (40 g SiO2, 30 to 100% EtOAc-hexane gradient elution) to afford 312 mg of tert-butyl (2-chloro-5-(difluoromethyl)-3-(4-(oxetan-3-yl)piperazin-1-yl)phenyl)(4-methoxybenzyl)carbamate.

後処理

  1. customthe reaction was degassed 3 times
  2. customby evacuating the flask under vacuum
  3. custompurging with N2
  4. temperaturecooled to room temperature
  5. additionThe reaction mixture was diluted with EtOAc
  6. customsonicated
  7. filtrationfiltered through celite
  8. concentrationconcentrated
  9. customThe product was purified by column chromatography (40 g SiO2, 30 to 100% EtOAc-hexane gradient elution)

出典と根拠

ORDレコード
ord-673badd90e754d49858ba4c5bf510bed
出典データセット
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09273057B2

反応ノート

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