Cysteamine Hydrochloride → HCID 15592296, compound

HRID 1075107Notes

Reaction equation

HRID 1075107 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]=1

Participants

4

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

  1. temperatureheated at an oil bath temperature of 100° for 96 hours
  2. customThe mixture was evaporated under reduced pressure
  3. extractionThe aqueous phase was extracted with methyl acetate
  4. customdried
  5. customevaporated

Sources & evidence

ORD record
ord-5b14669643704bc09cc59399b0639867
Source dataset
uspto-grants-1983_07
Patent number
US04394508

Reaction notes

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