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Diisopropylethylamine → Ethyl 3-(4-(2-carbamoylpyridin-4-yloxy)-3-fluorophenylamino)-3-oxopropanoate

HRID 2237278
ノート
印刷プレビュー

反応式

HRID 2237278 の反応式
[NH2:1][C:2]1[CH:17]=[CH:16][C:5]([O:6][C:7]2[CH:12]=[CH:11][N:10]=[C:9]([C:13]([NH2:15])=[O:14])[CH:8]=2)=[C:4]([F:18])[CH:3]=1.C(OC1C=CC(NC2N=CN=C(OC3C=CC(NC(=O)CC(NC4C=CC(F)=CC=4)=O)=CC=3F)C=2)=CC=1)C1C=CC=CC=1.CCN(C(C)C)C(C)C.Cl[C:72](=[O:79])[CH2:73][C:74]([O:76][CH2:77][CH3:78])=[O:75]>CN(C=O)C.CCOC(C)=O>[C:13]([C:9]1[CH:8]=[C:7]([O:6][C:5]2[CH:16]=[CH:17][C:2]([NH:1][C:72](=[O:79])[CH2:73][C:74]([O:76][CH2:77][CH3:78])=[O:75])=[CH:3][C:4]=2[F:18])[CH:12]=[CH:11][N:10]=1)(=[O:14])[NH2:15]
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 81531DiisopropylethylamineHCID 118931Ethyl 3-chloro-3-oxopropionate2 回HCID 231532054-(4-Amino-2-fluorophenoxy)picolinamideHCID 59853038N-(4-(6-(4-(Benzyloxy)phenylamino)pyrimidin-4-yloxy)-3-fluorophenyl)-N3-(4-fluorophenyl)malonamide

生成物 1

HCID 59853090Ethyl 3-(4-(2-carbamoylpyridin-4-yloxy)-3-fluorophenylamino)-3-oxopropanoate
収率 62%

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide溶媒HCID 8857Ethyl Acetate溶媒

実験手順

To a solution of 4-(4-amino-2-fluorophenoxy)picolinamide (Compound B′ of Example 24, 1.0 g, 4.0 mmol) in DMF (10.0 mL) were added DIEA (2.0 mL) and ethyl 3-chloro-3-oxopropanoate (Aldrich, 0.75 mL, 6.0 mmol). The mixture was stirred at room temperature for 12 h and more ethyl 3-chloro-3-oxopropanoate (0.20 mL, 1.6 mmol) was added. The mixture was stirred for 2 h and was then diluted with EtOAc (200 mL). It was washed with H2O and brine and then dried over MgSO4. After filtration and concentration, the residue was triturated with DCM and filtered to give ethyl 3-(4-(2-carbamoylpyridin-4-yloxy)-3-fluorophenylamino)-3-oxopropanoate (900 mg, 62% yield). MS(ESI+) m/z 362.28 (M+H)+.

後処理

  1. stirringThe mixture was stirred for 2 h
  2. washIt was washed with H2O and brine
  3. dry with materialdried over MgSO4
  4. filtrationAfter filtration and concentration
  5. customthe residue was triturated with DCM
  6. filtrationfiltered

出典と根拠

ORDレコード
ord-bf6a3c8ef6e948a6817386d8ca302795
出典データセット
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07714138B2

反応ノート

読み込み中…

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