Water → tert-Butyl 5-(2-trifluoromethylbenzoyl)-3,4,5,6-tetrahydro-1H-pyrrolo[3,4-c]pyrrole-2-carboxylate

HRID 1186775Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1186775
Cl.[CH2:2]1[C:6]2[CH2:7][NH:8][CH2:9][C:5]=2[CH2:4][N:3]1[C:10]([O:12][C:13]([CH3:16])([CH3:15])[CH3:14])=[O:11].C(N(CC)CC)C.[F:24][C:25]([F:36])([F:35])[C:26]1[CH:34]=[CH:33][CH:32]=[CH:31][C:27]=1[C:28](Cl)=[O:29].O>C(Cl)Cl>[F:24][C:25]([F:35])([F:36])[C:26]1[CH:34]=[CH:33][CH:32]=[CH:31][C:27]=1[C:28]([N:8]1[CH2:7][C:6]2[CH2:2][N:3]([C:10]([O:12][C:13]([CH3:16])([CH3:15])[CH3:14])=[O:11])[CH2:4][C:5]=2[CH2:9]1)=[O:29]

Komponenten

6

Versuchsvorschrift

tert-Butyl 3,4,5,6-tetrahydro-1H-pyrrolo[3,4-C]pyrrole-2-carboxylate hydrochloride (30 g, 121.6 mmol) was suspended in 700 ml of methylene chloride, triethylamine (50.7 ml, 364.8 mmol) was added with ice bath cooling, and 2-(trifluoromethyl)benzoyl chloride (25.22 ml, 171.2 mmol) was slowly added dropwise. The brown suspension was stirred for 2 h, in the course of which it was allowed to come to RT. The reaction mixture was admixed with water, and the organic phase was removed, dried and concentrated by rotary evaporation. The crude product (56.8 g) was converted further without purification.

Aufarbeitung

  1. temperaturecooling
  2. customto come to RT
  3. customthe organic phase was removed
  4. customdried
  5. concentrationconcentrated by rotary evaporation
  6. customThe crude product (56.8 g) was converted further without purification

Quellen und Nachweise

ORD-Eintrag
ord-c8919835bd52435098e98114a3b10906
Quelldatensatz
uspto-grants-2014_03
Patentnummer
US08673917B2

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