Hydrogen Sulfide → HCID 21319833, compound
Reaction equation
[CH2:1]([S:3][C:4]1[S:5][C:6]([C:10]#[N:11])=[C:7]([NH2:9])[N:8]=1)[CH3:2].[SH2:12]>>[CH2:1]([S:3][C:4]1[S:5][C:6]([C:10](=[S:12])[NH2:11])=[C:7]([NH2:9])[N:8]=1)[CH3:2]Participants
3
Procedure
55.5 parts of 2-ethylmercapto-4-amino-5-cyano-thiazole are reacted with 20 parts of hydrogen sulfide as described in Example 1(a). 32.1 parts of 2-ethylmercapto-4-amino-5-thiocarbamoylthiazole (49% of theory) of melting point 180°-183° C. are obtained.
Sources & evidence
- ORD record
- ord-7720ab5c38c345e1a628c45e0463fdf9
- Source dataset
- uspto-grants-1979_05
- Patent number
- US04153607
Reaction notes
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