Dimethylformamide → N-[3-[(4aR,7aS)-2-Amino-4a-fluoro-5,7-dihydro-4H-furo[3,4-d][1,3]oxazin-7 a-yl]-4-fluoro-phenyl]-5-chloro-pyrazine-2-carboxamide

HRID 571740ノート

反応式

HRID 571740 の反応式
[Cl:1][C:2]1[N:3]=[CH:4][C:5]([C:8]([OH:10])=O)=[N:6][CH:7]=1.C(#N)C.CN(C=O)C.C(Cl)(=O)C(Cl)=O.[NH2:25][C:26]1[CH:27]=[CH:28][C:29]([F:43])=[C:30]([C@:32]23[CH2:40][O:39][CH2:38][C@@:37]2([F:41])[CH2:36][O:35][C:34]([NH2:42])=[N:33]3)[CH:31]=1>C(OCC)(=O)C.O.C(O)C>[NH2:42][C:34]1[O:35][CH2:36][C@:37]2([F:41])[CH2:38][O:39][CH2:40][C@:32]2([C:30]2[CH:31]=[C:26]([NH:25][C:8]([C:5]3[CH:4]=[N:3][C:2]([Cl:1])=[CH:7][N:6]=3)=[O:10])[CH:27]=[CH:28][C:29]=2[F:43])[N:33]=1

参加物

9

反応物 5

HCID 6228DimethylformamideHCID 6342AcetonitrileHCID 65578Oxalyl chlorideHCID 4654725-Chloropyrazinoic acidHCID 117738453(4aR,7aS)-7a-(5-amino-2-fluoro-phenyl)-4a-fluoro-5,7-dihydro-4H-furo[3,4-d][1,3]oxazin-2-amine

生成物 1

HCID 117738587N-[3-[(4aR,7aS)-2-Amino-4a-fluoro-5,7-dihydro-4H-furo[3,4-d][1,3]oxazin-7 a-yl]-4-fluoro-phenyl]-5-chloro-pyrazine-2-carboxamide収率 94%

試薬・触媒・溶媒 3

HCID 702Ethanol溶媒HCID 962Water溶媒HCID 8857Ethyl Acetate溶媒

実験手順

Scheme 3, steps M, substep 2 or step N, substep 3 (amidation): A mixture of 5-chloropyrazine-2-carboxylic acid (1.53 g, 9.66 mmol) in acetonitrile (15 mL, 283 mmol) is treated with DMF (115 μL, 1.49 mmol) and oxalyl chloride (970 μL, 11.1 mmol). The mixture is stirred at ambient temperature under nitrogen for 20 minutes. In a separate flask is added (4aR,7aS)-7a-(5-amino-2-fluoro-phenyl)-4a-fluoro-5,7-dihydro-4H-furo[3,4-d][1,3]oxazin-2-amine (2.00 g, 7.43 mmol), ethanol (7.4 mL), water (7.4 mL) and the mixture is heated at 50° C. The acid chloride is added to the solution prepared above and the reaction mixture is stirred at 50° C. for 20 minutes. The reaction is cooled to room temperature, diluted with ethyl acetate (200 mL), and washed with water (40 mL) and saturated aqueous NaHCO3 (40 mL). The aqueous washes are combined and extracted with ethyl acetate (100 mL). The combined organic layers are dried (Na2SO4) and the solvent removed in vacuo to give the crude product. The crude product is purified by silica gel flash chromatography, eluting with ethyl acetate to give the title product (2.85 g, 94%). ES/MS (m/e): 410 (M+1)

後処理

  1. temperaturethe mixture is heated at 50° C
  2. customprepared above and the reaction mixture
  3. stirringis stirred at 50° C. for 20 minutes
  4. temperatureThe reaction is cooled to room temperature
  5. washwashed with water (40 mL) and saturated aqueous NaHCO3 (40 mL)
  6. extractionextracted with ethyl acetate (100 mL)
  7. dry with materialThe combined organic layers are dried (Na2SO4)
  8. customthe solvent removed in vacuo
  9. customto give the crude product
  10. customThe crude product is purified by silica gel flash chromatography
  11. washeluting with ethyl acetate

出典と根拠

ORDレコード
ord-bf033a5f5a0c488581907e42606c4e54
出典データセット
uspto-grants-2015_05
特許番号
US09029367B2

反応ノート

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