Acetonitrile → (S)-7-bromo-3-(difluoromethoxy)-2',6'-dihydrospiro[chromeno[2,3-c]pyridine-5,3'-[1,4]oxazin]-5'-amine

HRID 455672ノート

反応式

HRID 455672 の反応式
[NH2:1][C:2]1[CH2:7][O:6][CH2:5][C@:4]2([C:20]3[CH:19]=[C:18]([OH:21])[N:17]=[CH:16][C:15]=3[O:14][C:13]3[C:8]2=[CH:9][C:10]([Br:22])=[CH:11][CH:12]=3)[N:3]=1.[F-].[Cs+].C(#N)C.[F:28][C:29]([F:41])(S(F)(=O)=O)C(O[Si](C)(C)C)=O>CCOC(C)=O>[Br:22][C:10]1[CH:9]=[C:8]2[C@:4]3([N:3]=[C:2]([NH2:1])[CH2:7][O:6][CH2:5]3)[C:20]3[CH:19]=[C:18]([O:21][CH:29]([F:41])[F:28])[N:17]=[CH:16][C:15]=3[O:14][C:13]2=[CH:12][CH:11]=1

参加物

6

反応物 4

HCID 6342AcetonitrileHCID 25953Cesium fluorideHCID 2778022Trimethylsilyl 2,2-difluoro-2-(fluorosulfonyl)acetateHCID 178508236HCID 178508236、化合物

生成物 1

HCID 67438254(S)-7-bromo-3-(difluoromethoxy)-2',6'-dihydrospiro[chromeno[2,3-c]pyridine-5,3'-[1,4]oxazin]-5'-amine収率 19.7%

試薬・触媒・溶媒 1

HCID 8857Ethyl Acetate溶媒

実験手順

A flask was charged with (S)-5′-amino-7-bromo-2′,6′-dihydrospiro[chromeno[2,3-c]pyridine-5,3′-[1,4]oxazin]-3-ol (0.250 g, 0.690 mmol), cesium fluoride (9.17 mg, 0.069 mmol), and acetonitrile (6.90 mL). Trimethylsilyl 2,2-difluoro-2-(fluorosulfonyl)acetate (0.272 mL, 1.381 mmol) was added slowly and the reaction was stirred for 15 minutes. The reaction was diluted with EtOAc and washed with water. The aqueous layer was extracted with EtOAc, and the combined organic layers were washed with brine, dried with sodium sulfate, filtered, and concentrated. The material was purified via column chromatography (0-10% MeOH/DCM), to afford (S)-7-bromo-3-(difluoromethoxy)-2′,6′-dihydrospiro[chromeno[2,3-c]pyridine-5,3′-[1,4]oxazin]-5′-amine (0.056 g, 0.136 mmol, 19.68% yield) as a light yellow solid. [M+H]+=411.9

後処理

  1. washwashed with water
  2. extractionThe aqueous layer was extracted with EtOAc
  3. washthe combined organic layers were washed with brine
  4. dry with materialdried with sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe material was purified via column chromatography (0-10% MeOH/DCM)

出典と根拠

ORDレコード
ord-5f5fe5ee06204252bd93457ef2ed8611
出典データセット
uspto-grants-2013_07
特許番号
US08497264B2

反応ノート

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