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Dichloromethane → Tert-butyl 3-(6-chloropyridin-3-yl)azetidine-1-carboxylate

HRID 626758
ノート
印刷プレビュー

反応式

HRID 626758 の反応式
Cl[Si](C)(C)C.BrCCBr.[C:10]([O:14][C:15]([N:17]1[CH2:20][CH:19](I)[CH2:18]1)=[O:16])([CH3:13])([CH3:12])[CH3:11].C(Cl)Cl.[Cl:25][C:26]1[CH:31]=[C:30](I)[CH:29]=[CH:28][N:27]=1.IC1C=CC=CN=1>CC(N(C)C)=O.[Zn].C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2].[Cu](I)I>[C:10]([O:14][C:15]([N:17]1[CH2:20][CH:19]([C:29]2[CH:28]=[N:27][C:26]([Cl:25])=[CH:31][CH:30]=2)[CH2:18]1)=[O:16])([CH3:13])([CH3:12])[CH3:11]
参加物実験手順後処理出典と根拠反応ノート

参加物

11

反応物 6

HCID 6344DichloromethaneHCID 6397ChlorotrimethylsilaneHCID 78391,2-DibromoethaneHCID 2211262-IodopyridineHCID 15165112-Chloro-4-iodopyridineHCID 11000522Tert-butyl 3-iodoazetidine-1-carboxylate

生成物 1

HCID 57537370
Tert-butyl 3-(6-chloropyridin-3-yl)azetidine-1-carboxylate
収率 56%

試薬・触媒・溶媒 4

HCID 23994Zinc触媒2 回HCID 83717Copper iodide触媒HCID 44119782Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)触媒HCID 31374Dimethylacetamide溶媒3 回

実験手順

To a de-gassed suspension of zinc powder (912 mg, 14 mmol) in DMA (2.3 mL) was added drop-wise a solution of chlorotrimethylsilane and 1,2-dibromoethane (0.1 mL, 7:5 v/v ratio) and the resultant mixture was stirred at room temperature for 15 minutes. To this mixture was then added dropwise to a solution of 3-iodoazetidine-1-carboxylic acid tert-butyl ester (3.2 g, 11.3 mmol) in DMA (8.0 mL) and the resultant mixture was stirred at room temperature for 15 minutes. In a separate flask, PdCl2(dppf)2.DCM (196 mg, 0.24 mmol) and then copper iodide (92 mg, 0.48 mmol) were added to a degassed solution of 2-chloro-4-iodopyridine in DMA (20 mL). After allowing to age for 30 minutes, the zinc suspension above was added to the iodopyridine solution and the reaction mixture was allowed to stir at room temperature for 2 hours. The resultant mixture was quenched by adding saturated ammonium chloride solution and was then extracted with TBME (×2). The combined organic washings were dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by silica gel flash chromatography (0-25% ethyl acetate in cyclohexane) to afford the title compound as a white solid (1.2 g, 56%). LCMS (Method F): RT=3.71 min, m/z: 414 [M+H+].

後処理

  1. customThe resultant mixture was quenched
  2. additionby adding saturated ammonium chloride solution
  3. extractionwas then extracted with TBME (×2)
  4. dry with materialThe combined organic washings were dried over anhydrous sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure
  7. customThe residue was purified by silica gel flash chromatography (0-25% ethyl acetate in cyclohexane)

出典と根拠

ORDレコード
ord-e8e669af4a7948d993ebaee73706818d
出典データセット
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09309240B2

反応ノート

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