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Isopropylamine → 1,4-dichloro-6-isopropyl-6H-pyrrolo[3,4-d]pyridazine

HRID 42226
ノート
印刷プレビュー

反応式

HRID 42226 の反応式
Br[CH2:2][C:3]1[C:8]([CH2:9]Br)=[C:7]([Cl:11])[N:6]=[N:5][C:4]=1[Cl:12].C(=O)([O-])[O-].[Na+].[Na+].[CH:19]([NH2:22])([CH3:21])[CH3:20].CCCCCCC>C1COCC1.[I-].C([N+](CCCC)(CCCC)CCCC)CCC>[Cl:11][C:7]1[C:8]2=[CH:9][N:22]([CH:19]([CH3:21])[CH3:20])[CH:2]=[C:3]2[C:4]([Cl:12])=[N:5][N:6]=1
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 4

HCID 6363IsopropylamineHCID 8900HeptaneHCID 10340Sodium CarbonateHCID 574716294,5-Bis(bromomethyl)-3,6-dichloropyridazine

生成物 1

HCID 574716301,4-dichloro-6-isopropyl-6H-pyrrolo[3,4-d]pyridazine収率 58.2%

試薬・触媒・溶媒 2

HCID 67553
Tetrabutylammonium Iodide
触媒
HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
70 °C

実験手順

To a suspension of 4,5-bis(bromomethyl)-3,6-dichloropyridazine (700 mg, 2.09 mmol) in 66 mL anhydrous THF was added with sodium carbonate (443 mg, 4.18 mmol) and tetrabutylammonium iodide (77.2 mg, 0.21 mmol). The reaction mixture was added with isopropyl amine (0.18 mL, 2.09 mmol) in 10 mL THF dropwisely for 2 h. The reaction mixture was heated at 70° C. for 3 h. The reaction mixture was concentrated, dissolved in DCM and washed with water and brine. The organics solution was dried over Na2SO4 and concentrated to afford a crude oil. The mixture was purified by flash chromatography on silica gel, eluting with 10-80% EtOAc:heptane to afford a off-white solid (280 mg, yield: 47%).

後処理

  1. concentrationThe reaction mixture was concentrated
  2. dissolutiondissolved in DCM
  3. washwashed with water and brine
  4. dry with materialThe organics solution was dried over Na2SO4
  5. concentrationconcentrated
  6. customto afford a crude oil
  7. customThe mixture was purified by flash chromatography on silica gel
  8. washeluting with 10-80% EtOAc

出典と根拠

ORDレコード
ord-9441bd98ad47423c9bcb6f925b4f2f6c
出典データセット
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08536168B2

反応ノート

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