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Hydrogen Bromide → 2-Bromo-5-methyl-4,5,6,7-tetrahydrothiazolo(5,4-c)pyridine

HRID 557240
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 557240
N[C:2]1[S:3][C:4]2[CH2:5][N:6]([CH3:11])[CH2:7][CH2:8][C:9]=2[N:10]=1.[BrH:12].N([O-])=O.[Na+].[OH-].[Na+]>O>[Br:12][C:2]1[S:3][C:4]2[CH2:5][N:6]([CH3:11])[CH2:7][CH2:8][C:9]=2[N:10]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 260Hydrogen BromideHCID 14798Sodium HydroxideHCID 23979985-methyl-4H,5H,6H,7H-[1,3]thiazolo[5,4-c]pyridin-2-amineHCID 23668193Sodium Nitrite

Produkt 1

HCID 111723352-Bromo-5-methyl-4,5,6,7-tetrahydrothiazolo(5,4-c)pyridine

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962
Water
Lösungsmittel
2×

Reaktionsbedingungen

Temperatur
30 °C

Versuchsvorschrift

2-Amino-5-methyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine (600.0 g) was suspended in water (6.0 L), and 48% hydrobromic acid (4.2 L) was added dropwise thereto at 5 to 15° C. A solution of sodium nitrite (367.2 g) in water (1.8 L) was added dropwise thereto at 0 to 5° C. over 1.5 hours, and the reaction mixture was heated to 30° C., followed by stirring for 24 hours. The resultant mixture was made strongly basic (pH 12.5) with 5N aqueous sodium hydroxide (6.0 L). The aqueous layer was extracted with toluene twice (12.0 L, 6.0 L), and the toluene layers were combined. The combined toluene layer was dried over sodium sulfate anhydrate (1202.0 g), and after any insoluble material was filtered off, the mother liquor was concentrated at 40° C. under reduced pressure, to thereby give 557.6 g of the title compound.

Aufarbeitung

  1. customat 5 to 15° C
  2. extractionThe aqueous layer was extracted with toluene twice (12.0 L, 6.0 L)
  3. dry with materialThe combined toluene layer was dried over sodium sulfate anhydrate (1202.0 g)
  4. filtrationafter any insoluble material was filtered off
  5. concentrationthe mother liquor was concentrated at 40° C. under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-75ba8a71c6724b758b23d5cbec286bb8
Quelldatensatz
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08058440B2

Notizen zur Reaktion

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