Phenylacetic Acid → 5-(4-fluorophenyl)-2-isopropyl-1-(3-morpholin-4-yl-3-oxo-propyl)-4-phenyl-1H-pyrrole-3-carboxylic acid phenylamide

HRID 351456ノート

反応式

HRID 351456 の反応式
[NH2:1][CH2:2][CH2:3][C:4]([N:6]1[CH2:11][CH2:10][O:9][CH2:8][CH2:7]1)=[O:5].C1(CC(O)=O)C=CC=CC=1.[C:22]1([NH:28][C:29](=[O:52])[CH:30]([CH:36]([C:46]2[CH:51]=[CH:50][CH:49]=[CH:48][CH:47]=2)[C:37]([C:39]2[CH:44]=[CH:43][C:42]([F:45])=[CH:41][CH:40]=2)=O)[C:31](=O)[CH:32]([CH3:34])[CH3:33])[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1>C1COCC1>[C:22]1([NH:28][C:29]([C:30]2[C:36]([C:46]3[CH:47]=[CH:48][CH:49]=[CH:50][CH:51]=3)=[C:37]([C:39]3[CH:40]=[CH:41][C:42]([F:45])=[CH:43][CH:44]=3)[N:1]([CH2:2][CH2:3][C:4]([N:6]3[CH2:11][CH2:10][O:9][CH2:8][CH2:7]3)=[O:5])[C:31]=2[CH:32]([CH3:34])[CH3:33])=[O:52])[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1

参加物

5

反応物 3

HCID 999Phenylacetic AcidHCID 65042503-Amino-1-(morpholin-4-yl)propan-1-oneHCID 99098724-(4-Fluorophenyl)-2-(2-methyl-1-oxopropyl)-4-oxo-3,N-diphenylbutanamide

生成物 1

HCID 111919355-(4-fluorophenyl)-2-isopropyl-1-(3-morpholin-4-yl-3-oxo-propyl)-4-phenyl-1H-pyrrole-3-carboxylic acid phenylamide

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

A nitrogen inerted reactor, equipped with a suitable reflux condenser and soxhlet extractor containing freshly activated 3A molecular sieves (4–8 mesh; 97.2 g), is charged with 3-amino-1-morpholin-4-yl-propan-1-one, compound with phenylacetic acid (765 mmol) and 2-[2-(4-fluorophenyl)-2-oxo-1-phenyl-ethyl]-4-methyl-3-oxo-pentanoic acid phenylamide (450 mmol). THF (360 mL) is added, and the resulting solution is stirred vigorously as the reaction is heated at reflux temperature for ca. 24 hours, during which time the product begins to precipitate. Half-saturated aqueous NaHCO3 (100 mL) is added, and the reaction mixture is cooled with continued stirring to ca. 0° C. MtBE (100 mL) is added, and the solids are collected via filtration. The solid is washed with distilled water (100 mL) and MtBE (2×100 mL), collected, and dried under vacuum at <50° C. to afford 5-(4-fluorophenyl)-2-isopropyl-1-(3-morpholin-4-yl-3-oxo-propyl)-4-phenyl-1H-pyrrole-3-carboxylic acid phenylamide as a white solid (194 g). This material is carried on to subsequent steps without further purification.

後処理

  1. customA nitrogen inerted reactor, equipped with a suitable reflux condenser
  2. additionsoxhlet extractor containing freshly
  3. temperatureis heated
  4. temperatureat reflux temperature for ca. 24 hours
  5. customto precipitate
  6. additionHalf-saturated aqueous NaHCO3 (100 mL) is added
  7. temperaturethe reaction mixture is cooled
  8. stirringwith continued stirring to ca. 0° C
  9. additionMtBE (100 mL) is added
  10. filtrationthe solids are collected via filtration
  11. washThe solid is washed with distilled water (100 mL) and MtBE (2×100 mL)
  12. customcollected
  13. customdried under vacuum at <50° C.

出典と根拠

ORDレコード
ord-0cef5dcfe9dd4520a861542a2effa154
出典データセット
uspto-grants-2007_02
特許番号
US07183408B2

反応ノート

読み込み中…