Acetic Acid → 3-[5-(2-Chloro-4-pyrimidinyl)-2-(1-methylethyl)-1,3-thiazol-4-yl]-2-(methyloxy)aniline

HRID 590121ノート

反応式

HRID 590121 の反応式
C(OC(=O)[NH:6][C:7]1[CH:12]=[CH:11][CH:10]=[C:9]([C:13]2[N:14]=[C:15]([CH:25]([CH3:27])[CH3:26])[S:16][C:17]=2[C:18]2[CH:23]=[CH:22][N:21]=[C:20]([Cl:24])[N:19]=2)[C:8]=1[O:28][CH3:29])C=C.C(O)(=O)C.C([SnH](CCCC)CCCC)CCC>C(Cl)Cl.Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1>[Cl:24][C:20]1[N:19]=[C:18]([C:17]2[S:16][C:15]([CH:25]([CH3:27])[CH3:26])=[N:14][C:13]=2[C:9]2[C:8]([O:28][CH3:29])=[C:7]([CH:12]=[CH:11][CH:10]=2)[NH2:6])[CH:23]=[CH:22][N:21]=1

参加物

6

反応物 3

HCID 176Acetic AcidHCID 5948TributylstannaneHCID 579896912-Propen-1-yl[3-[5-(2-chloro-4-pyrimidinyl)-2-(1-methylethyl)-1,3-thiazol-4-yl]-2-(methyloxy)phenyl]carbamate

生成物 1

HCID 579898673-[5-(2-Chloro-4-pyrimidinyl)-2-(1-methylethyl)-1,3-thiazol-4-yl]-2-(methyloxy)aniline収率 123.2%

試薬・触媒・溶媒 2

HCID 178418476HCID 178418476、化合物触媒HCID 6344Dichloromethane溶媒

実験手順

To the solution of 2-propen-1-yl[3-[5-(2-chloro-4-pyrimidinyl)-2-(1-methylethyl)-1,3-thiazol-4-yl]-2-(methyloxy)phenyl]carbamate (12.1 g, 22.5 mmol) in DCM (200 mL), acetic acid (3.8 mL, 66.6 mmol), Pd(PPh3)2Cl2 (0.45 g, 0.56 mmol) were added. Then tri-n-butyl tin hydride (8.5 mL, 33 mmol) was added dropwise to the mixture at 0° C. The mixture was stirred at rt for 30 min. The reaction was quenched by added the saturated NaHCO3 (200 mL) slowly. The two layers were separated. The aqueous layer was extracted with DCM (200 mL×2). The combined organic layers were washed with water and brine successively, dried over Na2SO4, filtered and concentrated under reduced pressure to give the crude product, which was washed with petroleum ether (500 mL) to afford the title compound of Step G (10 g, 60.8% yield), which was used directly in the next step.

後処理

  1. customThe reaction was quenched
  2. additionby added the saturated NaHCO3 (200 mL) slowly
  3. customThe two layers were separated
  4. extractionThe aqueous layer was extracted with DCM (200 mL×2)
  5. washThe combined organic layers were washed with water and brine successively
  6. dry with materialdried over Na2SO4
  7. filtrationfiltered
  8. concentrationconcentrated under reduced pressure
  9. customto give the crude product, which
  10. washwas washed with petroleum ether (500 mL)

出典と根拠

ORDレコード
ord-ac60338ade0d491888d745283742737b
出典データセット
uspto-grants-2016_01
特許番号
US09233956B2

反応ノート

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