Hydrazine → HCID 12370274, compound

HRID 2083031Notes

Reaction equation

HRID 2083031 reaction equation
[F:1][S:2]([O-:5])(=[O:4])=[O:3].[Cl:6][C:7]1[CH:12]=[CH:11][C:10]([N+:13]2[CH:18]=[CH:17][C:16](OC)=[CH:15][CH:14]=2)=[CH:9][CH:8]=1.[NH2:21][NH2:22]>CO>[F:1][S:2]([OH:5])(=[O:4])=[O:3].[Cl:6][C:7]1[CH:12]=[CH:11][C:10]([N:13]2[CH:18]=[CH:17][C:16](=[N:21][NH2:22])[CH:15]=[CH:14]2)=[CH:9][CH:8]=1

Participants

4

Reactant 2

HCID 9321HydrazineHCID 12370270HCID 12370270, compound

Product 1

HCID 12370274HCID 12370274, compound

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

To a suspension of 3.2 g. (0.01 mole) of 1-(4-chlorophenyl)-4-methoxypyridinium fluorosulfonate, prepared by the process set forth in Example 1, in 20 ml. methanol was added 0.4 g. anhydrous hydrazine. The mixture was heated to boiling for a few minutes and the resulting clear orange solution was kept overnight at room temperature. The product, in the form of orange crystals, was obtained in two crops. The total weight was 2.97 g. (93%). The product was recrystallized from methanol, m.p. 174°-176° C. The elemental analyses for C, H, N and Cl were within ±0.4% of the theoretical values.

Workup

  1. additionTo a suspension of 3.2 g
  2. temperatureThe mixture was heated
  3. waitto boiling for a few minutes
  4. customThe product, in the form of orange crystals, was obtained in two crops
  5. customThe product was recrystallized from methanol, m.p. 174°-176° C

Sources & evidence

ORD record
ord-8d15f49b3a2b427fa0734ecda167d36a
Source dataset
uspto-grants-1978_04
Patent number
US04083984

Reaction notes

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