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Sodium Hydroxide → HCID 44606816, 화합물

HRID 1372574
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HRID 1372574 반응식
[F:1][C:2]1[C:10]2[O:9][C:8]([NH:11][C:12]3[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=3[CH3:18])=[N:7][C:6]=2[CH:5]=[CH:4][C:3]=1[CH2:19][C:20]([O:22]C)=[O:21].[OH-].[Na+]>C1COCC1>[F:1][C:2]1[C:10]2[O:9][C:8]([NH:11][C:12]3[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=3[CH3:18])=[N:7][C:6]=2[CH:5]=[CH:4][C:3]=1[CH2:19][C:20]([OH:22])=[O:21]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 58778451Methyl 7-fluoro-2-(2-methylphenylamino)-6-benzoxazolylacetate

생성물 1

HCID 44606816HCID 44606816, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

Methyl 7-fluoro-2-(2-methylphenylamino)-6-benzoxazolylacetate (1.31 g, 4.17 mmol) was dissolved in THF (30 ml), followed by the addition of 0.25N NaOH (30 ml). The resulting mixture was stirred at room temperature for 20 hours. The reaction mixture was distilled under reduced pressure to remove the solvent. The residue was acidified with 1N HCl, followed by extraction with a chloroform/methanol (10/1) mixture. The extract was washed with saturated brine, dried over anhydrous sodium sulfate and distilled under reduced pressure to remove the solvent, whereby the title compound (1.08 g, 86%) was obtained as a pale brown solid.

후처리

  1. distillationThe reaction mixture was distilled under reduced pressure
  2. customto remove the solvent
  3. extractionfollowed by extraction with a chloroform/methanol (10/1) mixture
  4. washThe extract was washed with saturated brine
  5. dry with materialdried over anhydrous sodium sulfate
  6. distillationdistilled under reduced pressure
  7. customto remove the solvent, whereby the title compound (1.08 g, 86%)
  8. customwas obtained as a pale brown solid

출처 및 근거

ORD 기록
ord-b0cd3d13784d44589152c1dad6b10ce4
출처 데이터셋
uspto-grants-2007_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07157487B2

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