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Ammonia → HCID 18180211, compound

HRID 1383310
Notes
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Reaction equation

HRID 1383310 reaction equation
Cl[C:2]1[C:7]([Br:8])=[N:6][CH:5]=[C:4]([NH2:9])[N:3]=1.[NH3:10]>C(O)C>[NH2:10][C:2]1[C:7]([Br:8])=[N:6][CH:5]=[C:4]([NH2:9])[N:3]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 222AmmoniaHCID 181802075-Bromo-6-chloropyrazin-2-amine

Product 1

HCID 18180211HCID 18180211, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Conditions

Temperature
160 °C

Procedure

A suspension of 2-chloro-3-bromo-6-aminopyrazine (15 g, 0.072 mole) in absolute ethanol (150 ml) and 0.880 ammonia (375 ml) was stirred and heated in an autoclave at 160° C. and 20 atm. for 16 hrs. The cooled mixture was evaporated in vacuo and extracted with hot methanol (3×100 ml). The combined methanol extracts were evaporated in vacuo. The residue was dissolved in hot chloroform, dried over anhydrous magnesium sulphate, filtered and the filtrate evaporated in vacuo. The residue was triturated with 40-60° C. petroleum ether, filtered, and dried in vacuo. Yield 5.51 g (40%), M.p. 176-178° C.

Workup

  1. customThe cooled mixture was evaporated in vacuo
  2. extractionextracted with hot methanol (3×100 ml)
  3. customThe combined methanol extracts were evaporated in vacuo
  4. dissolutionThe residue was dissolved in hot chloroform
  5. dry with materialdried over anhydrous magnesium sulphate
  6. filtrationfiltered
  7. customthe filtrate evaporated in vacuo
  8. customThe residue was triturated with 40-60° C. petroleum ether
  9. filtrationfiltered
  10. customdried in vacuo

Sources & evidence

ORD record
ord-984a243b4b0a42e5828df20265ddba3d
Source dataset
uspto-grants-2001_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06255307B1

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes