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Dichloromethane → 6-chloro-1-(1S)-camphanoyl-4-cyclopropylethynyl-4-trifluoromethyl-1,4-dihydro-2H-3,1-benzoxazin-2-one

HRID 1376437
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Reaktionsgleichung

Reaktionsgleichung von HRID 1376437
ClC1[CH:3]=[CH:4][C:5]2[N:10](C#C)[C:9](=[O:13])[O:8][C:7]([CH:18]3[CH2:20][CH2:19]3)([C:14]([F:17])([F:16])[F:15])[C:6]=2[CH:21]=1.[C:22]12([CH3:34])[C:28]([CH3:30])([CH3:29])[CH:25]([CH2:26][CH2:27]1)[CH2:24][CH:23]2[C:31](Cl)=[O:32].[CH2:35](N(CC)CC)[CH3:36].Cl[CH2:43][Cl:44]>CN(C)C1C=CN=CC=1>[Cl:44][C:43]1[CH:3]=[CH:4][C:5]2[N:10]([C:31]([CH:23]3[CH2:24][CH:25]4[C:28]([CH3:30])([CH3:29])[C@@:22]3([CH3:34])[CH2:27][CH2:26]4)=[O:32])[C:9](=[O:13])[O:8][C:7]([C:18]#[C:19][CH:20]3[CH2:36][CH2:35]3)([C:14]([F:17])([F:16])[F:15])[C:6]=2[CH:21]=1
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Komponenten

6

Edukt 4

HCID 6344DichloromethaneHCID 8471TriethylamineHCID 534427834,7,7-Trimethyl-3-bicyclo[2.2.1]heptanecarbonyl chlorideHCID 54382198(+/-) 6-chloro-4-cyclopropyl-ethynyl-4-trifluoromethyl-1,4-dihydro-2H-3,1-benzoxazin-2-one

Produkt 1

HCID 702720696-chloro-1-(1S)-camphanoyl-4-cyclopropylethynyl-4-trifluoromethyl-1,4-dihydro-2H-3,1-benzoxazin-2-one

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 142844-(Dimethylamino)pyridineKatalysator

Versuchsvorschrift

To a solution containing (±) 6-chloro-4-cyclopropyl-ethynyl-4-trifluoromethyl-1,4-dihydro-2H-3,1-benzoxazin-2-one (12.97 g, 0.041 mol), 4-dimethylaminopyridine (1.02 g, 0.0083 mol), and (-) camphanic acid chloride (14.22 g, 0.06556 mol) in 350 mL of dry dichloromethane, stirred under argon in an ice bath, was added triethylamine (22.84 mL, 0.164 mol). The cooling bath was removed and the reaction was allowed to proceed at room temperature. After 75 min. the reaction was judged complete by thin layer chromatography (SiO2, 4% EtOAc in CHCl3), and the solution was diluted with 500 mL of CHCl3 then washed with 10% citric acid (2X), water (1X), and brine (1X). Drying (MgSO4), filtration, and removal of the solvent in vacuo left a colorless foam. This material was triturated with 200 mL of boiling hexane. On cooling to room temperature the desired diastereomeric camphanate imide precipitated. The solid was collected on a frit, washed with a little cold hexanes and dried in vacuo to give 7.79g of 6-chloro-1-(1S) -camphanoyl-4-cyclopropylethynyl-4-trifluoromethyl-1,4-dihydro-2H-3,1-benzoxazin-2-one as white crystals. mp: 164°-165° C. HPLC purity: 99.2% @254 nm. 1H-NMR (CDCl3): δ0.77 (s, 3H), 0.86-0.96 (m, 4H), 1.08 (s, 3H), 1.19 (s, 3H), 1.44 (m, 1H), 1.76 (m, 1H), 1.95 (m, 1H), 2.51 (m, 2H), 7.42 (dd, J=2.4,9.0 Hz, 1H), 7.63 (m, 2H).

Aufarbeitung

  1. customThe cooling bath was removed
  2. customto proceed at room temperature
  3. additionthe solution was diluted with 500 mL of CHCl3
  4. washthen washed with 10% citric acid (2X), water (1X), and brine (1X)
  5. customDrying
  6. filtration(MgSO4), filtration, and removal of the solvent in vacuo
  7. waitleft a colorless foam
  8. customThis material was triturated with 200 mL of boiling hexane
  9. customprecipitated
  10. customThe solid was collected on a frit
  11. washwashed with a little cold hexanes
  12. customdried in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-5aade1dcc06f4c7283639125154afd65
Quelldatensatz
uspto-grants-1997_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05663169

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