Hydrochloric Acid → HCID 58490209, compound

HRID 1395871Notes

Reaction equation

HRID 1395871 reaction equation
Cl.O[CH2:3][CH2:4][C:5](=[NH:9])OCC.[N:10]1[CH:15]=[CH:14][CH:13]=[N:12][C:11]=1[C:16]#[N:17].[OH2:18].[NH2:19][NH2:20].N([O-])=O.[Na+].Cl>O>[N:10]1[CH:15]=[CH:14][CH:13]=[N:12][C:11]=1[C:16]1[N:17]=[N:9][C:5]([CH2:4][CH2:3][OH:18])=[N:20][N:19]=1

Participants

7

Reactant 5

HCID 313Hydrochloric AcidHCID 24654Hydrazine hydrate (1:1)HCID 27579792-CyanopyrimidineHCID 12653320HCID 12653320, compoundHCID 23668193Sodium Nitrite

Product 1

HCID 58490209HCID 58490209, compound

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Conditions

Temperature
90 °C

Procedure

To a mixture of ethyl 3-hydroxypropanimidate hydrochloride (1 mmol, 153 mg) and 2-Pyrimidinecarbonitrile (5 mmol, 525 mg) was added hydrazine hydrate (1 mL). After stirring at 90° C. for 1 hour, the mixture was cooled, diluted with water (10 mL), filtered, and to the filtrate was added sodium nitrite (10 mmol, 0.69 g) with stirring. To this pink solution was added 2% aqueous HCl dropwise on an ice bath until the solution reached a pH of 3. The solution was dried by rotary evaporation, the residue was washed with methanol (2×10 mL), filtered, and the filtrate was dried by rotary evaporation. Column chromatography on silica gel eluting with 1.5% methanol in methylene chloride afforded pure 2-(6-(pyrimidin-2-yl)-1,2,4,5-tetrazin-3-yl)ethanol (26 mg, 12.7%), as a pink solid. LRMS-ESI [M+H]+ calcd. for C8H9N6O+: 205.08, found: 204.9.

Workup

  1. temperaturethe mixture was cooled
  2. filtrationfiltered
  3. stirringwith stirring
  4. customThe solution was dried by rotary evaporation
  5. washthe residue was washed with methanol (2×10 mL)
  6. filtrationfiltered
  7. customthe filtrate was dried by rotary evaporation

Sources & evidence

ORD record
ord-8cf022a2a8854a7e92558b1c75f6f242
Source dataset
uspto-grants-2014_12
Patent number
US08900549B2

Reaction notes

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