HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2171782Generated: November 1, 2026
Methanesulfonyl chloride → [2-(4,4-Dimethylcyclohexyl)-5-methyl[1,3]thiazolo[5,4-d]pyrimidin-7-yl]methyl methanesulfonate
https://huagongshe.com/reaction/2171782
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 118023489 | HCID 118023489 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | [2-(4,4-Dimethylcyclohexyl)-5-methyl[1,3]thiazolo[5,4-d]pyrimidin-7-yl]methyl methanesulfonate | HCID 118023977 | — |
Reaction Steps
To a mixture of [2-(4,4-dimethylcyclohexyl)-5-methyl[1,3]thiazolo[5,4-d]pyrimidin-7-yl]methanol (6.42 g) and EtOAc (65 mL) were added dropwise TEA (4.5 mL) and MsCl (2.1 mL) under ice-cooling, followed by stirring at 0° C. for 1 hour. The reaction mixture was filtered and then to the liquid was added saturated aqueous sodium bicarbonate, followed by extraction with EtOAc. The organic layer was dried over MgSO4 and then concentrated under reduced pressure to obtain [2-(4,4-dimethylcyclohexyl)-5-methyl[1,3]thiazolo[5,4-d]pyrimidin-7-yl]methyl methanesulfonate (9.3 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09051339B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-906161eebe484381a6d936a629ee837c |
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| Source note | uspto-grants-2015_06 |
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