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Hydrochloric Acid → Methyl (S)-2-(Boc-amino)-4-iodobutanoate

HRID 1755489
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1755489
[NH2:1][C@@H:2]([CH2:7][CH2:8]Br)[C:3]([O:5][CH3:6])=[O:4].Cl.C(N(CC)C(C)C)(C)C.[C:20]([O:24][C:25]([O:27]C(OC(C)(C)C)=O)=O)([CH3:23])([CH3:22])[CH3:21].[I-:35].[Na+]>C1COCC1>[C:20]([O:24][C:25]([NH:1][C@@H:2]([CH2:7][CH2:8][I:35])[C:3]([O:5][CH3:6])=[O:4])=[O:27])([CH3:23])([CH3:22])[CH3:21]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 5

HCID 313Hydrochloric AcidHCID 5238Sodium IodideHCID 81531DiisopropylethylamineHCID 90495Di-tert-butyl dicarbonateHCID 1512645(S)-methyl 2-amino-4-bromobutanoate

Produkt 1

HCID 14394150Methyl (S)-2-(Boc-amino)-4-iodobutanoateAusbeute 60 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel2×

Versuchsvorschrift

To an ice cold suspension of (S)-methyl 2-amino-4-bromobutanoate, 1.00 HCl (see WO2003/101948 A2, 4.42 g, 19.02 mmol) and N,N-diisopropylethylamine (9.97 mL, 57.1 mmol) in anhydrous THF (50 mL) is slowly added a solution of di-tert-butyldicarbonate (4.36 g, 19.97 mmol) in anhydrous THF (8 mL). The reaction is stirred for 18 h while warming to room temp. The solvent is removed in vacuo, and the residue is partitioned between EtOAc (450 mL) and aqueous saturated ammonium chloride (30 ml). The organic layer is washed with aqueous saturated sodium bicarbonate (1×30 mL), water (1×30 mL), brine (1×30 mL), dried over Na2SO4, filtered and evaporated to dryness. The residue is dissolved in acetone (450 mL). treated with sodium iodide (14.25 g, 95.1 mmol) and the reaction is refluxed for 18 h. The reaction is cooled to room temp, filtered thru a ground glass frit and the solvent removed in vacuo. The residue is dissolved in EtOAc (450 mL), washed with water (3×40 mL), brine (1×40 mL), dried over Na2SO4, filtered, evaporated to dryness and purified by BIOTAGE® Silica gel chromatography on a 80 g Thompson Single Step silica cartridge using 100% CH2Cl2 over 10 column volumes to give 3.9 g (60%) of the title compound as a thick oil. LC/MS (Condition A): ret. T=3.40 min, (M+Na) 366.

Aufarbeitung

  1. customThe solvent is removed in vacuo
  2. customthe residue is partitioned between EtOAc (450 mL) and aqueous saturated ammonium chloride (30 ml)
  3. washThe organic layer is washed with aqueous saturated sodium bicarbonate (1×30 mL), water (1×30 mL), brine (1×30 mL)
  4. dry with materialdried over Na2SO4
  5. filtrationfiltered
  6. customevaporated to dryness
  7. dissolutionThe residue is dissolved in acetone (450 mL)
  8. temperaturethe reaction is refluxed for 18 h
  9. temperatureThe reaction is cooled to room temp
  10. filtrationfiltered thru a ground glass frit
  11. customthe solvent removed in vacuo
  12. dissolutionThe residue is dissolved in EtOAc (450 mL)
  13. washwashed with water (3×40 mL), brine (1×40 mL)
  14. dry with materialdried over Na2SO4
  15. filtrationfiltered
  16. customevaporated to dryness
  17. custompurified by BIOTAGE® Silica gel chromatography on a 80 g Thompson Single Step silica cartridge

Quellen und Nachweise

ORD-Eintrag
ord-989fdc351bbd4fd887b5c4b420ca943b
Quelldatensatz
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09169295B2

Notizen zur Reaktion

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