Hydrochloric Acid → HCID 178503294, compound
Reaction equation
[CH3:1][S:2][C:3](SC)=[C:4]([C:7]#[N:8])[C:5]#[N:6].[C:11]([CH2:13][C:14]([NH2:16])=[S:15])#[N:12].C(N(CC)CC)C.Cl>CN(C=O)C>[NH2:8][C:7]1[C:4]([C:5]#[N:6])=[C:3]([S:2][CH3:1])[C:13]([C:11]#[N:12])=[C:14]([SH:15])[N:16]=1Participants
6
Procedure
10 g (58.74 mmol) of 2-(di(methylthio))methylidenemalononitrile and 7.1 g (70.48 mmol) of cyanothioacetamide were initially charged in 21 ml of DMF, and 16.4 ml (117.47 mmol) of triethylamine were added dropwise at room temperature. The mixture was stirred at room temperature for 8 h. The reaction mixture was added to 300 ml of 3N hydrochloric acid. The resulting precipitate was filtered off with suction, washed with water and dried. This gave the product as a powder.
Workup
- filtrationThe resulting precipitate was filtered off with suction
- washwashed with water
- customdried
Sources & evidence
- ORD record
- ord-e9140ad50a22404b94914cac713dc37a
- Source dataset
- uspto-grants-2013_12
- Patent number
- US08609686B2
Reaction notes
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