Cysteamine Hydrochloride → HCID 15592296, compound
Reaction equation
Cl.[NH2:2][CH2:3][CH2:4][SH:5].Cl.[CH3:7][N:8]([CH3:16])[C:9]1[S:10][CH:11]=[C:12]([CH2:14]Cl)[N:13]=1>Cl>[CH3:7][N:8]([CH3:16])[C:9]1[S:10][CH:11]=[C:12]([CH2:14][S:5][CH2:4][CH2:3][NH2:2])[N:13]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Cysteamine hydrochloride (5.24 g; 45.9 mmoles) and 2-dimethylamino-4-chloromethylthiazole hydrochloride (9.8 g; 45.9 mmoles) [prepared from N,N-dimethylthiourea and 1,3-dichloro-2-propanone] were dissolved in 45 ml of concentrated hydrochloric acid and heated at an oil bath temperature of 100° for 96 hours. The mixture was evaporated under reduced pressure and the residue made basic with 40% aqueous NaOH. The aqueous phase was extracted with methyl acetate, dried and evaporated to give the title compound as an oil which was used without further purification in Step B.
Workup
- temperatureheated at an oil bath temperature of 100° for 96 hours
- customThe mixture was evaporated under reduced pressure
- extractionThe aqueous phase was extracted with methyl acetate
- customdried
- customevaporated
Sources & evidence
- ORD record
- ord-ad31555cefa4426f882479080874e3af
- Source dataset
- uspto-grants-1985_04
- Patent number
- US04510309
Reaction notes
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