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Cesium fluoride → 2-cyclopropyl-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid ((S)-1-dimethylcarbamoyl-ethyl)-amide

HRID 446951
ノート
印刷プレビュー

反応式

HRID 446951 の反応式
[CH:1]1([C:4]2[N:5]=[C:6]3[C:12]([C:13]([NH:15][C@@H:16]([CH3:22])[C:17]([N:19]([CH3:21])[CH3:20])=[O:18])=[O:14])=[CH:11][N:10](COCC[Si](C)(C)C)[C:7]3=[N:8][CH:9]=2)[CH2:3][CH2:2]1.C1OCCOCCOCCOCCOCCOC1.[F-].[Cs+]>C(#N)C>[CH3:21][N:19]([CH3:20])[C:17]([C@@H:16]([NH:15][C:13]([C:12]1[C:6]2[C:7](=[N:8][CH:9]=[C:4]([CH:1]3[CH2:2][CH2:3]3)[N:5]=2)[NH:10][CH:11]=1)=[O:14])[CH3:22])=[O:18]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 25953Cesium fluorideHCID 2855718-Crown-6HCID 67388122(S)-2-cyclopropyl-N-(1-(dimethylamino)-1-oxopropan-2-yl)-5-((2-(trimethyl-silyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxamide

生成物 1

HCID 533898222-cyclopropyl-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid ((S)-1-dimethylcarbamoyl-ethyl)-amide収率 48%

試薬・触媒・溶媒 1

HCID 6342
Acetonitrile
溶媒

実験手順

To a solution of (S)-2-cyclopropyl-N-(1-(dimethylamino)-1-oxopropan-2-yl)-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxamide (150 mg, 0.35 mmol) in acetonitrile (15.8 mL) at room temperature was added 18-crown-6 (92 mg, 0.35 mmol) and cesium fluoride (528 mg, 3.48 mmol). The reaction mixture was heated to reflux temperature for 48 h then cooled to room temperature and filtered over a pad of celite. The filtrate was evaporated under vacuum and the crude residue was partitioned between EtOAc (25 mL) and water (25 mL). The organic extract was dried (Na2SO4) and evaporated under vacuum. The crude residue was purified by preparative TLC (CH2Cl2/MeOH/NH4OH, 90:9.5:0.5) to give 48 mg (48%) of 2-cyclopropyl-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid ((S)-1-dimethylcarbamoyl-ethyl)-amide as an off-white solid. MS: (M+H)+=302.

後処理

  1. temperatureThe reaction mixture was heated
  2. temperatureto reflux temperature for 48 h
  3. filtrationfiltered over a pad of celite
  4. customThe filtrate was evaporated under vacuum
  5. customthe crude residue was partitioned between EtOAc (25 mL) and water (25 mL)
  6. extractionThe organic extract
  7. dry with materialwas dried (Na2SO4)
  8. customevaporated under vacuum
  9. customThe crude residue was purified by preparative TLC (CH2Cl2/MeOH/NH4OH, 90:9.5:0.5)

出典と根拠

ORDレコード
ord-9c685fc84c984a5389615b4668b1f49c
出典データセット
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08481541B2

反応ノート

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