Cesium carbonate → HCID 68816272、化合物

HRID 735020ノート

反応式

HRID 735020 の反応式
C(=O)([O-])[O-].[Cs+].[Cs+].I[C:8]1[CH:13]=[CH:12][C:11]([C:14]2([NH:17][C:18](=[O:24])[O:19][C:20]([CH3:23])([CH3:22])[CH3:21])[CH2:16][CH2:15]2)=[CH:10][CH:9]=1.[Cl:25][C:26]1[CH:31]=[CH:30][C:29]([C:32]2[CH:37]=[CH:36][C:35]([NH:38][C:39](=[O:42])[C:40]#[CH:41])=[CH:34][CH:33]=2)=[CH:28][CH:27]=1>C1COCC1.[Cu]I>[Cl:25][C:26]1[CH:27]=[CH:28][C:29]([C:32]2[CH:37]=[CH:36][C:35]([NH:38][C:39](=[O:42])[C:40]#[C:41][C:8]3[CH:13]=[CH:12][C:11]([C:14]4([NH:17][C:18]([O:19][C:20]([CH3:23])([CH3:22])[CH3:21])=[O:24])[CH2:16][CH2:15]4)=[CH:10][CH:9]=3)=[CH:34][CH:33]=2)=[CH:30][CH:31]=1

参加物

6

実験手順

1.4 g (4.2 mmol) of cesium carbonate and 0.5 g (1.4 mmol) of tert-butyl [1-(4-iodophenyl)cyclopropyl]carbamate are placed in 20 mL of THF and cooled to −15° C. in the ice/methanol bath, rinsed with argon, and degassed. To this reaction mixture is added successively 160 mg (0.14 mmol) of tetrakistriphenylphosphine palladium and 30 mg (0.158 mmol) of copper (I) iodide and the mixture is again degassed. 0.5 g (1.4 mmol) of propynoic acid-(4′-chlorobiphenyl-4-yl)amide is finally added. The mixture is stirred for 24 hours at ambient temperature and the reaction mixture is then evaporated down. The residue is triturated with water and ethyl acetate, suction filtered, washed with ethyl acetate, and dried in the air. Yield: 0.4 g (59% of theory); C29H27ClN2O3 (M=486.99); calc.: molecular ion peak (M+H)+: 487/89 (Cl); found: molecular ion peak (M+H)+: 487/89 (Cl); Rf value: 0.62 (silica gel, cyclohexane/ethyl acetate (1:1)).

後処理

  1. washrinsed with argon
  2. customdegassed
  3. customthe mixture is again degassed
  4. customthe reaction mixture is then evaporated down
  5. customThe residue is triturated with water and ethyl acetate, suction
  6. filtrationfiltered
  7. washwashed with ethyl acetate
  8. customdried in the air

出典と根拠

ORDレコード
ord-7827551ac0e84c6aa6b7c7dbc7a85bef
出典データセット
uspto-grants-2009_09
特許番号
US07592373B2

反応ノート

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