Potassium Carbonate → 1-methyl-5-(2-oxo-1,2-dihydrospiro [3,1-benzoxazine-4,1'-cyclobutan]-6-yl)-1H-pyrrole-2-carbonitrile

HRID 915896ノート

反応式

HRID 915896 の反応式
[CH3:1][N:2]1[CH:6]=[CH:5][CH:4]=[C:3]1[C:7]#[N:8].C(OB(OC(C)C)OC(C)C)(C)C.C([N-]C(C)C)(C)C.[Li+].Br[C:31]1[CH:32]=[CH:33][C:34]2[NH:43][C:42](=[O:44])[O:41][C:37]3([CH2:40][CH2:39][CH2:38]3)[C:35]=2[CH:36]=1.C(=O)([O-])[O-].[K+].[K+].[Cl-].[NH4+]>C1COCC1.O>[CH3:1][N:2]1[C:6]([C:31]2[CH:32]=[CH:33][C:34]3[NH:43][C:42](=[O:44])[O:41][C:37]4([CH2:40][CH2:39][CH2:38]4)[C:35]=3[CH:36]=2)=[CH:5][CH:4]=[C:3]1[C:7]#[N:8]

参加物

9

実験手順

To a solution of 1-methyl-1H-pyrrole-2-carbonitrile (0.84 g, 7.1 mmol) and triisopropylborate (1.8 mL, 7.8 mmol) in THF (15 mL) at 0° C. was added lithium diisopropylamide (4.6 mL, 9.2 mmol). The reaction was allowed to warm to room temperature. Upon completion by TLC, the reaction was added dropwise to a 65° C. solution of 6-bromospiro[3,1-benzoxazine-4,1′-cyclobutan]-2(1H)-one (0.38 g, 1.4 mmol), potassium carbonate (0.58 g, 4.2 mmol) dissolved in (5 mL water), and tetrakistriphenylphosphine palladium (0) (0.081 g, 0.07 mmol) in tetrahydrofuran (10 mL). Upon completion by TLC of the reaction the reaction mixture was poured into a saturated solution of ammonium chloride (100 mL), extracted with ethyl acetate (50 mL), dried with magnesium sulfate, and purified on a silica gel column (40% ethyl acetate/hexane) to give 1-methyl-5-(2-oxo-1,2-dihydrospiro[3,1-benzoxazine-4,1′-cyclobutan]-6-yl)-1H-pyrrole-2-carbonitrile (0.33 g, 79%) as a light red solid. 1H NMR (DMSO-d6): δ 10.41 (s, 1H), 7.58 (d, 1H, J=2 Hz), 7.43 (dd, 1H, J=8.2, 1.8 Hz), 7.04 (d, 1H, J=4.0 Hz), 6.39 (d, 1H, J=8.2 Hz), 6.39 (d, 1H, J=4.0 Hz), 3.73 (s, 3H), 2.55-2.49 (m, 2H), 2.05-1.90 (m, 2H), 1.88-1.83 (m, 2H). MS (ESI) m/z 294 ([M+H]+); MS (ESI) m/z 292 ([M−H]−). High resolution mass spectrometry (HRMS): calcd for C17H15N3O2, 293.1164; found (ESI_FT), 294.12311.

後処理

  1. customUpon completion by TLC of the reaction the reaction mixture
  2. extractionextracted with ethyl acetate (50 mL)
  3. dry with materialdried with magnesium sulfate
  4. custompurified on a silica gel column (40% ethyl acetate/hexane)

出典と根拠

ORDレコード
ord-28a12cc7ef4f4d18b0c593656d240a26
出典データセット
uspto-grants-2007_09
特許番号
US07268149B2

反応ノート

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