Potassium Hydroxide → HCID 178479424, compound
Reaction equation
S(O)(O)(=O)=O.CS[C:8](=[NH:10])[NH2:9].[OH-].[K+].[NH2:13][CH2:14][C:15]1[NH:20][C:19](=[O:21])[NH:18][C:17](=[O:22])[C:16]=1[Cl:23]>>[ClH:23].[Cl:23][C:16]1[C:17](=[O:22])[NH:18][C:19](=[O:21])[NH:20][C:15]=1[CH2:14][NH:13][C:8]([NH2:10])=[NH:9]Participants
4
Conditions
- Temperature
- 80 °C
Procedure
Subsequent to addition of 455 mg of 2-methyl-isothiourea sulfate to 33 ml of a 0.1 N aqueous solution of potassium hydroxide under ice cooling, 600 mg of the 6-aminomethyl-5-chlorouracil obtained in Example 22 were added, followed by heating for 2 hours at 80° C. under stirring. After the reaction mixture was allowed to cool down, a crystallized matter was collected by filtration and washed with 2 N hydrochloric acid, whereby 287 mg of the title compound were obtained (yield: 33%).
Workup
- temperatureto cool down
- filtrationa crystallized matter was collected by filtration
- washwashed with 2 N hydrochloric acid
Sources & evidence
- ORD record
- ord-4bef7d86dba743ed81a383dcec08127f
- Source dataset
- uspto-grants-2001_07
- Patent number
- US06255314B1
Reaction notes
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