4-Morpholinepropanoic acid, methyl ester → 3-Morpholino-N-(2-phenylbenzo[d]oxazol-5-yl)propanamide

HRID 1896748

反応式

HRID 1896748 の反応式
[C:1]1([C:7]2[O:8][C:9]3[CH:15]=[CH:14][C:13]([NH2:16])=[CH:12][C:10]=3[N:11]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[O:17]1[CH2:22][CH2:21][N:20]([CH2:23][CH2:24][C:25](OC)=[O:26])[CH2:19][CH2:18]1.C[Al](C)C.C(=O)(O)[O-].[Na+]>C1(C)C=CC=CC=1>[O:17]1[CH2:22][CH2:21][N:20]([CH2:23][CH2:24][C:25]([NH:16][C:13]2[CH:14]=[CH:15][C:9]3[O:8][C:7]([C:1]4[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=4)=[N:11][C:10]=3[CH:12]=2)=[O:26])[CH2:19][CH2:18]1

参加物

6

反応条件

温度
160 °C

実験手順

To 2-phenylbenzo[d]oxazol-5-amine (75 mg, 0.36 mmol) and methyl 3-morpholinopropanoate (63 μL, 0.39 mmol) in toluene (2.5 mL) was added a 2M solution of trimethylaluminum in toluene (0.22 mL, 0.43 mmol). The resulting solution was heated twice for 5 min at 160° C. in the microwave. After cooling, sodium bicarbonate solution was added and the aqueous layer was extracted with ethyl acetate. The organic layer was then washed with brine and the combined organic layers were dried over anhydrous MgSO4. After evaporation, the impurities were removed by filtering through on a plug of silica eluting with ethyl acetate/hexanes 50:50 v/v and the desired product was obtained by elution with methanol to afford 17.5 mg (14%) of the title compound (LCMS RT=5.54 min, MH+ 352.0)

後処理

  1. temperatureAfter cooling
  2. extractionthe aqueous layer was extracted with ethyl acetate
  3. washThe organic layer was then washed with brine
  4. dry with materialthe combined organic layers were dried over anhydrous MgSO4
  5. customAfter evaporation
  6. customthe impurities were removed
  7. filtrationby filtering through on a plug of silica eluting with ethyl acetate/hexanes 50:50 v/v

出典と根拠

ORDレコード
ord-65df4c1dc796480bb495e12218559b3e
出典データセット
uspto-grants-2013_08
特許番号
US08518980B2

関連ノート

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