Hydrochloric Acid → 2-[7-Bromo-3-(4-bromo-2-fluorobenzyl)-1,2,3,4-tetrahydro-2,4-dioxoquinazolin-1-yl]acetic acid

HRID 1639316

反応式

HRID 1639316 の反応式
[Br:1][C:2]1[CH:11]=[C:10]2[C:5]([C:6](=[O:28])[N:7]([CH2:19][C:20]3[CH:25]=[CH:24][C:23]([Br:26])=[CH:22][C:21]=3[F:27])[C:8](=[O:18])[N:9]2[CH2:12][C:13]([O:15]CC)=[O:14])=[CH:4][CH:3]=1.[OH-].[Na+].Cl>CO>[Br:1][C:2]1[CH:11]=[C:10]2[C:5]([C:6](=[O:28])[N:7]([CH2:19][C:20]3[CH:25]=[CH:24][C:23]([Br:26])=[CH:22][C:21]=3[F:27])[C:8](=[O:18])[N:9]2[CH2:12][C:13]([OH:15])=[O:14])=[CH:4][CH:3]=1

参加物

5

反応物 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 14458963Ethyl 2-[7-bromo-3-(4-bromo-2-fluorobenzyl)-1,2,3,4-tetrahydro-2,4-dioxoquinazolin-1-yl]acetate

生成物 1

HCID 144238012-[7-Bromo-3-(4-bromo-2-fluorobenzyl)-1,2,3,4-tetrahydro-2,4-dioxoquinazolin-1-yl]acetic acid収率 83.2%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

A solution of ethyl 2-[7-bromo-3-(4-bromo-2-fluorobenzyl)-1,2,3,4-tetrahydro-2,4-dioxoquinazolin-1-yl]acetate (3.0 g) and 1N aqueous sodium hydroxide (5.83 ml) in methanol (69.6 ml) was refluxed for 1 hour with stirring. After cooling, the solvent was evaporated to give a residue, which was acidified with 1N aqueous hydrochloric acid and extracted with ethyl acetate. The extract was washed with brine and dried. Removal of the solvent gave a residue, which was recrystallized from a mixture of ethyl acetate and n-hexane to afford 2-[7-bromo-3-(4-bromo-2-fluorobenzyl)-1,2,3,4-tetrahydro-2,4-dioxoquinazolin-1-yl]acetic acid (2.36 g).

後処理

  1. temperatureAfter cooling
  2. customthe solvent was evaporated
  3. customto give a residue, which
  4. extractionextracted with ethyl acetate
  5. washThe extract was washed with brine
  6. customdried
  7. customRemoval of the solvent
  8. customgave a residue, which
  9. customwas recrystallized from a mixture of ethyl acetate and n-hexane

出典と根拠

ORDレコード
ord-2986f6a7aa954e62a52089d0daa9aa46
出典データセット
uspto-grants-1989_11
特許番号
US04883800

関連ノート

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