Ethanethiol → HCID 13336875, compound
Reaction equation
[C:1]([C:3]1[C:8]([C:9]#[N:10])=[N:7][C:6](Cl)=[C:5]([CH3:12])[N:4]=1)#[N:2].[CH2:13]([SH:15])[CH3:14].[OH-].[Na+]>>[C:1]([C:3]1[C:8]([C:9]#[N:10])=[N:7][C:6]([S:15][CH2:13][CH3:14])=[C:5]([CH3:12])[N:4]=1)#[N:2]Participants
4
Procedure
2,3-Dicyano-5-chloro-6-methylpyrazine (1.79 g; 0.01 mole), 0.62 g (0.01 mole) of ethanethiol and 0.40 g (0.01 mole) of sodium hydroxide were worked up in the same way as in Example 8. Recrystallization from ethanol afforded 0.91 g (yield 45%) of 2,3-dicyano-5-ethylthio-6-methylpyrazine.
Workup
- customRecrystallization from ethanol
Sources & evidence
- ORD record
- ord-8e34c42eb7994a84976a28b6aeb1d464
- Source dataset
- uspto-grants-1984_07
- Patent number
- US04460403
Reaction notes
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