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Sodium borohydride → 1-[2-(3,4-dimethoxyphenyl)-2-hydroxyethyl]-4-(3,4-dihydro-2,2-dioxo-1H-2,1,3-benzothiadiazin-3-yl)-piperidine

HRID 2166891
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2166891
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:27]=[CH:28][C:29]=1[O:30][CH3:31])[C:6]([CH2:8][N:9]1[CH2:14][CH2:13][CH:12]([N:15]2[CH2:20][C:19]3[CH:21]=[CH:22][CH:23]=[CH:24][C:18]=3[NH:17][S:16]2(=[O:26])=[O:25])[CH2:11][CH2:10]1)=[O:7].[BH4-].[Na+]>CO>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:6]([OH:7])[CH2:8][N:9]2[CH2:10][CH2:11][CH:12]([N:15]3[CH2:20][C:19]4[CH:21]=[CH:22][CH:23]=[CH:24][C:18]=4[NH:17][S:16]3(=[O:25])=[O:26])[CH2:13][CH2:14]2)[CH:27]=[CH:28][C:29]=1[O:30][CH3:31]
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Komponenten

4

Edukt 2

HCID 4311764Sodium borohydride2×HCID 130521741-(3,4-dimethoxybenzoylmethyl)-4-(3,4-dihydro-2,2-dioxo-1H-2,1,3-benzothiadiazin-3-yl)-piperidine

Produkt 1

HCID 130521751-[2-(3,4-dimethoxyphenyl)-2-hydroxyethyl]-4-(3,4-dihydro-2,2-dioxo-1H-2,1,3-benzothiadiazin-3-yl)-piperidineAusbeute 65,6 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

In 150 ml of methanol, 2.2 g of 1-(3,4-dimethoxybenzoylmethyl)-4-(3,4-dihydro-2,2-dioxo-1H-2,1,3-benzothiadiazin-3-yl)-piperidine is suspended. While this suspension is stirred at room temperature, 1.0 g of sodium borohydride is added thereto by portions over a period of four hours. The mixture is stirred overnight at room temperature and 400 mg of sodium borohydride is added thereto. Then, the mixture is stirred overnight. The reaction solution is concentrated under reduced pressure. The residue is mixed with 100 ml of water and adjusted to pH 9.3 with concentrated hydrochloric acid. The resultant mixture is extracted with chloroform. The organic layer is washed with water, dried and freed from the solvent by distillation to obtain a syrup as a residue. This residue is crystallized by adding methanol thereto. The crystals are separated by filtration to obtain 1.93 g of crude crystals. The crude crystals are recrystallized from ethanol to obtain 1.45 g of 1-[2-(3,4-dimethoxyphenyl)-2-hydroxyethyl]-4-(3,4-dihydro-2,2-dioxo-1H-2,1,3-benzothiadiazin- 3-yl)-piperidine (Compound No. 10).

Aufarbeitung

  1. stirringThe mixture is stirred overnight at room temperature
  2. stirringThen, the mixture is stirred overnight
  3. concentrationThe reaction solution is concentrated under reduced pressure
  4. additionThe residue is mixed with 100 ml of water
  5. extractionThe resultant mixture is extracted with chloroform
  6. washThe organic layer is washed with water
  7. customdried
  8. distillationfreed from the solvent by distillation
  9. customto obtain a syrup as a residue
  10. customThis residue is crystallized
  11. additionby adding methanol
  12. customThe crystals are separated by filtration
  13. customto obtain 1.93 g of crude crystals
  14. customThe crude crystals are recrystallized from ethanol

Quellen und Nachweise

ORD-Eintrag
ord-e551d9639522418c97afe8fc5f7346c8
Quelldatensatz
uspto-grants-1983_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04390536

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