2,4-Dichloro-5-(trifluoromethyl)pyrimidine → (R)-tert-butyl 1-(4-(4-chloro-5-(trifluoromethyl)pyrimidin-2-ylamino)phenyl)ethylcarbamate

HRID 2077063

反応式

HRID 2077063 の反応式
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([C@H:8]([NH:10][C:11](=[O:17])[O:12][C:13]([CH3:16])([CH3:15])[CH3:14])[CH3:9])=[CH:4][CH:3]=1.Cl[C:19]1[N:24]=[C:23]([Cl:25])[C:22]([C:26]([F:29])([F:28])[F:27])=[CH:21][N:20]=1>ClCCCl.CC(O)(C)C.[Zn+2].[Br-].[Br-]>[Cl:25][C:23]1[C:22]([C:26]([F:28])([F:27])[F:29])=[CH:21][N:20]=[C:19]([NH:1][C:2]2[CH:7]=[CH:6][C:5]([C@H:8]([NH:10][C:11](=[O:17])[O:12][C:13]([CH3:16])([CH3:15])[CH3:14])[CH3:9])=[CH:4][CH:3]=2)[N:24]=1

参加物

5

反応物 2

HCID 27827742,4-Dichloro-5-(trifluoromethyl)pyrimidineHCID 10633571(R)-[1-(4-Amino-phenyl)-ethyl]-carbamic acid tert-butyl ester

生成物 1

HCID 57584789(R)-tert-butyl 1-(4-(4-chloro-5-(trifluoromethyl)pyrimidin-2-ylamino)phenyl)ethylcarbamate

試薬・触媒・溶媒 2

HCID 10421208Zinc bromide触媒HCID 21868497Tert-butyl alcohol 1,2-dichloroethane溶媒

反応条件

温度
25 °C

実験手順

C2 (690 mg, 2.92 mmol) was dissolved in 10 mL DCE:t-BuOH (1:1 vol:vol), and the resultant solution was treated with ZnBr2 (1.97 g, 8.76 mmol) and 2,4-dichloro-5-(trifluoromethyl)pyrimidine (748 mg, 3.45 mmol). The resultant mixture was then treated drop-wise with TEA (406 ml, 2.92 mmol), and the mixture was allowed to stir at 25° C. for about 20 hours. The reaction mixture was concentrated, and the resultant residue was treated with EtOAc. The resultant solution was washed with water and brine, and dried over MgSO4. The mixture was then filtered, concentrated, and purified by column chromatography eluting with 22% EtOAc/Heptane. The product-containing eluents were combined and concentrated to provide C3 as a white solid. Yield: 680 mg, 56%. MS− 415.2. 1H NMR (500 MHz, DMSO) δ: 10.59 (s, 1H), 8.74 (s, 1H), 7.53 (d, 2H), 7.31 (d, 1H), 7.23 (d, 2H), 4.54 (m, 1H), 1.33 (s, 9H), 1.25 (d, 3H).

後処理

  1. concentrationThe reaction mixture was concentrated
  2. additionthe resultant residue was treated with EtOAc
  3. washThe resultant solution was washed with water and brine
  4. dry with materialdried over MgSO4
  5. filtrationThe mixture was then filtered
  6. concentrationconcentrated
  7. custompurified by column chromatography
  8. washeluting with 22% EtOAc/Heptane
  9. concentrationconcentrated

出典と根拠

ORDレコード
ord-d399acda7f1b413597d5d9f225454820
出典データセット
uspto-grants-2011_04
特許番号
US07928109B2

関連ノート

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