Methylamine → HCID 178485044, compound
Reaction equation
[NH:1]([C:5]1[S:6][CH:7]=[C:8]([CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][NH:15][C:16](=[N:19][C:20]#[N:21])SC)[N:9]=1)[C:2]([NH2:4])=[NH:3].[CH3:22][NH2:23]>C(O)C>[NH:1]([C:5]1[S:6][CH:7]=[C:8]([CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][NH:15][C:16]([NH:23][CH3:22])=[N:19][C:20]#[N:21])[N:9]=1)[C:2]([NH2:4])=[NH:3]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 2-guanidino-4-[5-(3-cyano-2-methylisothioureido)pentyl]thiazole in ethanol was added ethanolic methylamine (33% w/v, 15 ml.). The mixture was allowed to stand overnight and then evaporated to dryness. The residue was crystallized from acetonitrile to give 2-guanidino-4-[5-(2-cyano-3-methylguanidino)pentyl]thiazole, m.p. 109°-113° C.
Workup
- customevaporated to dryness
- customThe residue was crystallized from acetonitrile
Sources & evidence
- ORD record
- ord-1ad39bef956b4808a7dae585d71e453d
- Source dataset
- uspto-grants-1980_11
- Patent number
- US04234735
Reaction notes
Loading…