Acetyl chloride → HCID 86737682, compound
Reaction equation
[Cl:1][C:2]1[N:7]=[C:6]([CH2:8][C:9]([N:11](F)[N:12](F)F)=[O:10])[CH:5]=[CH:4][CH:3]=1.C(Cl)(=O)C>>[Cl:1][C:2]1[N:7]=[C:6]([CH2:8][C:9]([NH:11][NH2:12])=[O:10])[CH:5]=[CH:4][CH:3]=1Participants
3
Procedure
A 4.3 g. portion of 2-chloro-6-hydrazinopyridine (prepared in Example 1) is treated with acetyl chloride by the procedure of Example 2. The reaction mixture is evaporated to dryness and the solid is treated with a saturated aqueous solution of sodium bicarbonate and filtered to yield 5.33 g. of crude product. The material is recrystallized from acetone to yield 3.70 g. of the product of the Example m.p. 220°-225° C.
Workup
- customThe reaction mixture is evaporated to dryness
- additionthe solid is treated with a saturated aqueous solution of sodium bicarbonate
- filtrationfiltered
- customto yield 5.33 g
- customThe material is recrystallized from acetone
- customto yield 3.70 g
Sources & evidence
- ORD record
- ord-f93596d351fb4d6fb6decdcda25a7887
- Source dataset
- uspto-grants-1981_04
- Patent number
- US04260767
Reaction notes
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