Stannous chloride dihydrate → 5-Hydrazinyl-2-methoxypyridine hydrochloride

HRID 1437202Notes

Reaction equation

HRID 1437202 reaction equation
[N:1]([O-])=O.[Na+].[NH2:5][C:6]1[CH:7]=[CH:8][C:9]([O:12][CH3:13])=[N:10][CH:11]=1.O.O.[Sn](Cl)[Cl:17]>O.Cl>[ClH:17].[NH:5]([C:6]1[CH:7]=[CH:8][C:9]([O:12][CH3:13])=[N:10][CH:11]=1)[NH2:1]

Participants

6

Procedure

A solution of sodium nitrite (3.795 g) in water (20 mL) was added dropwise to 5-amino-2-methoxypyridine (6.21 g) in concentrated hydrochloric acid (50 mL) over a period of 60 minutes with ice cooling, and the resultant mixture was stirred at a constant temperature for 30 minutes. Tin(II) chloride dihydrate (39.5 g) in concentrated hydrochloric acid (30 mL) was added dropwise to the reaction mixture at an internal temperature of about 10° C. for 30 minutes, followed by stirring for 2 hours at room temperature. Under cooling with ice, the reaction mixture was partitioned between sodium hydroxide (75 g) in water (300 mL) and diethyl ether. The aqueous layer was extracted with diethyl ether twice. Subsequently, the aqueous layer was saturated with sodium chloride, followed by extraction with diethyl ether. The organic layers were combined, and dried over sodium sulfate anhydrate, followed by filtration. 1M HCl in ethanol (50 mL) was added to the filtrate and the mixture was stirred. The solid that precipitated was collected by filtration, washed with diethyl ether, and dried, to thereby give the title compound (5.02 g, 57%).

Workup

  1. temperatureUnder cooling with ice
  2. customthe reaction mixture was partitioned between sodium hydroxide (75 g) in water (300 mL) and diethyl ether
  3. extractionThe aqueous layer was extracted with diethyl ether twice
  4. extractionfollowed by extraction with diethyl ether
  5. dry with materialdried over sodium sulfate anhydrate
  6. filtrationfollowed by filtration
  7. addition1M HCl in ethanol (50 mL) was added to the filtrate
  8. stirringthe mixture was stirred
  9. customThe solid that precipitated
  10. filtrationwas collected by filtration
  11. washwashed with diethyl ether
  12. customdried

Sources & evidence

ORD record
ord-b742d4cc98e24df6829bb3c7407bd661
Source dataset
uspto-grants-2009_11
Patent number
US07622471B2

Reaction notes

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