Sodium → HCID 178512599, compound
Reaction equation
Br.Br[CH2:3][C:4]1[CH:5]=[CH:6][C:7]2[S:11][C:10]([NH:12][C:13]([NH2:15])=[NH:14])=[N:9][C:8]=2[CH:16]=1.[Na]>>[NH2:9][CH2:8][CH2:7][S:11][CH2:3][C:4]1[CH:5]=[CH:6][C:7]2[S:11][C:10]([NH:12][C:13]([NH2:15])=[NH:14])=[N:9][C:8]=2[CH:16]=1Participants
3
Procedure
Cysteamine.hydrochloride (0.4 g) was caused to react with sodium ethoxide in ethanol to yield a sodium salt. Then, 5-bromomethyl-2-guanidinobenzothiazole.hydrobromide (0.63 g) was added to the sodium salt at an internal temperature of 0° C. After agitating the mixture over one night at room temperature, the solvent was removed, and the residue was made acidic with addition of dilute hydrochloric acid. The crystalline precipitate was collected to obtain 5-[(2-aminoethyl)thiomethyl]-2-guanidinobenzothiazole.2hydrochloride (0.5 g).
Workup
- customthe solvent was removed
- additionthe residue was made acidic with addition of dilute hydrochloric acid
- customThe crystalline precipitate was collected
Sources & evidence
- ORD record
- ord-5a7c41eac8dc4520adb61cd63edf6204
- Source dataset
- uspto-grants-1985_10
- Patent number
- US04550118
Reaction notes
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