Ammonia → tert-Butyl [(3S,5S,6S,8S)-8-[(3-amino-2,2-dimethyl-3-oxopropyl)carbamoyl]-6-hydroxy-3-{[4-methoxy-3-(3-methoxypropoxy)phenyl]methyl}-2,9-dimethyldecan-5-yl]carbamate

HRID 500015Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 500015
[C:1]([O:5][C:6]([N:8]1[C@H:12]([C@@H:13]([OH:29])[CH2:14][C@H:15]([C:19](=[O:28])[NH:20][CH2:21][C:22]([C:25](=[O:27])[NH2:26])([CH3:24])[CH3:23])[CH:16]([CH3:18])[CH3:17])[CH2:11][C@@H:10]([CH:30]([CH3:32])[CH3:31])[C@@H:9]1[C:33]1[CH:38]=[CH:37][C:36]([O:39][CH3:40])=[C:35]([O:41][CH2:42][CH2:43][CH2:44][O:45][CH3:46])[CH:34]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2].N.[Li].[Cl-].[NH4+]>O1CCCC1.C(O)C>[C:1]([O:5][C:6](=[O:7])[NH:8][C@@H:12]([CH2:11][C@H:10]([CH2:9][C:33]1[CH:38]=[CH:37][C:36]([O:39][CH3:40])=[C:35]([O:41][CH2:42][CH2:43][CH2:44][O:45][CH3:46])[CH:34]=1)[CH:30]([CH3:32])[CH3:31])[C@@H:13]([OH:29])[CH2:14][C@H:15]([C:19](=[O:28])[NH:20][CH2:21][C:22]([C:25](=[O:27])[NH2:26])([CH3:23])[CH3:24])[CH:16]([CH3:17])[CH3:18])([CH3:2])([CH3:3])[CH3:4]

Komponenten

7

Edukt 4

HCID 222AmmoniaHCID 25517Ammonium ChlorideHCID 3028194LithiumHCID 11998976HCID 11998976, Verbindung

Produkt 1

HCID 53348234tert-Butyl [(3S,5S,6S,8S)-8-[(3-amino-2,2-dimethyl-3-oxopropyl)carbamoyl]-6-hydroxy-3-{[4-methoxy-3-(3-methoxypropoxy)phenyl]methyl}-2,9-dimethyldecan-5-yl]carbamate

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 702EthanolLösungsmittelHCID 8028TetrahydrofuranLösungsmittel

Reaktionsbedingungen

Temperatur
-78 °C

Versuchsvorschrift

A solution of 0.037 g of amide 12 is dissolved in 1 mL of tetrahydrofurane and cooled to −78° C. Liquid ammonia is added followed by 0.0042 g of lithium metal. The deep blue solution is stirred for 2 hours at −78° C., and then 0.35 g of ethanol is added and the mixture is stirred for 30 minutes at −78° C. Ammonium chloride (0.15 g) is added and the mixture is warmed to room temperature. The organic phase is partitioned between water and ethyl acetate. The organic phase is separated and the solvent removed in vacuum. The residue is stirred with heptane and filtered. Removal of the heptane produces 13 identical with an authentic sample. M++H=652

Aufarbeitung

  1. stirringthe mixture is stirred for 30 minutes at −78° C
  2. temperaturethe mixture is warmed to room temperature
  3. customThe organic phase is partitioned between water and ethyl acetate
  4. customThe organic phase is separated
  5. customthe solvent removed in vacuum
  6. stirringThe residue is stirred with heptane
  7. filtrationfiltered
  8. customRemoval of the heptane

Quellen und Nachweise

ORD-Eintrag
ord-b182b95923df444ab9c555312d15ff6e
Quelldatensatz
uspto-grants-2010_08
Patentnummer
US07767831B2

Notizen zur Reaktion

Wird geladen…