HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424658Generated: October 29, 2026
Water → N-(2-(Benzylthio)-6-{[2-hydroxy-1-(hydroxymethyl)ethyl]amino}-pyrimidin-4-yl)methanesulfonamide
https://huagongshe.com/reaction/424658
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Serinol | HCID 68294 | — |
| Reactant | N-{2-(Benzylthio)-6-[(2-hydroxyethyl)amino]pyrimidin-4-yl}methanesulfonamide | HCID 57833129 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | N-(2-(Benzylthio)-6-{[2-hydroxy-1-(hydroxymethyl)ethyl]amino}-pyrimidin-4-yl)methanesulfonamide | HCID 57833152 | — |
Reaction Steps
To a solution of the subtitle product of Example 19 step (0.20 g) in NMP (0.5 ml) was added 2-aminopropane-1,3-diol (1.0 g) and the reaction was heated at 100° C. for 2 days. To the reaction was added EtOAc (50 ml) and H2O (50 ml). The organic layer was separated and washed with H2O (2×20 ml) and brine (20 ml). The organic layer was dried (MgSO4) and the solvent removed under reduced pressure to give a solid. This was purified by column chromatography (1:1 EtOAc/iso-hexane then EtOAc) to give the title compound as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08106063B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-3d463039994d4b47855cc94ff8534a7f |
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| Source note | uspto-grants-2012_01 |
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