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Dimethylformamide → (S)-2'-(cyclopropylethynyl)-7'-(2-methoxy-2-methylpropoxy)-5H-spiro[oxazole-4,9'-xanthen]-2-amine

HRID 335769
ノート
印刷プレビュー

反応式

HRID 335769 の反応式
[NH2:1][C:2]1[O:3][CH2:4][C@:5]2([N:25]=1)[C:18]1[CH:17]=[C:16]([C:19]#[C:20][CH:21]3[CH2:23][CH2:22]3)[CH:15]=[CH:14][C:13]=1[O:12][C:11]1[C:6]2=[CH:7][C:8]([OH:24])=[CH:9][CH:10]=1.C(=O)([O-])[O-].[Cs+].[Cs+].CN(C=O)C.I[CH2:38][C:39]([O:42][CH3:43])([CH3:41])[CH3:40]>O.CCOC(C)=O>[CH:21]1([C:20]#[C:19][C:16]2[CH:15]=[CH:14][C:13]3[O:12][C:11]4[C:6](=[CH:7][C:8]([O:24][CH2:38][C:39]([O:42][CH3:43])([CH3:41])[CH3:40])=[CH:9][CH:10]=4)[C@:5]4([CH2:4][O:3][C:2]([NH2:1])=[N:25]4)[C:18]=3[CH:17]=2)[CH2:23][CH2:22]1
参加物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 6228DimethylformamideHCID 10796Cesium carbonateHCID 189668321-Iodo-2-methoxy-2-methylpropaneHCID 67240959(S)-2-amino-2'-(cyclopropylethynyl)-5H-spiro[oxazole-4,9'-xanthen]-7'-ol

生成物 1

HCID 58466161(S)-2'-(cyclopropylethynyl)-7'-(2-methoxy-2-methylpropoxy)-5H-spiro[oxazole-4,9'-xanthen]-2-amine

試薬・触媒・溶媒 2

HCID 962
Water
溶媒
HCID 8857Ethyl Acetate溶媒

実験手順

A 2-5 mL microwave vial was charged with (S)-2-amino-2′-(cyclopropylethynyl)-5H-spiro[oxazole-4,9′-xanthen]-7′-ol (0.250 g, 0.752 mmol), cesium carbonate (0.980 g, 3.01 mmol), and DMF (3.01 mL). The mixture was stirred vigorously for 5 min, then 1-iodo-2-methoxy-2-methylpropane (0.303 mL, 2.257 mmol) was added via syringe. The vial was sealed and the reaction was microwaved at 110° C. for two hours. The mixture was diluted with water and EtOAc and the layers were separated, and the aqueous layer was extracted twice with EtOAc. The combined organic extracts were dried over sodium sulfate, filtered, and evaporated. The residue was purified by chromatography on a 12-g Redi-Sep column, eluting with 0-10% MeOH/DCM to provide (S)-2′-(cyclopropylethynyl)-7′-(2-methoxy-2-methylpropoxy)-5H-spiro[oxazole-4,9′-xanthen]-2-amine as an off-white solid.

後処理

  1. customThe vial was sealed
  2. customthe reaction was microwaved at 110° C. for two hours
  3. customthe layers were separated
  4. extractionthe aqueous layer was extracted twice with EtOAc
  5. dry with materialThe combined organic extracts were dried over sodium sulfate
  6. filtrationfiltered
  7. customevaporated
  8. customThe residue was purified by chromatography on a 12-g Redi-Sep column
  9. washeluting with 0-10% MeOH/DCM

出典と根拠

ORDレコード
ord-829e75c3867b4877988f7abf68a58a28
出典データセット
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08883782B2

反応ノート

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