HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 76179Generated: October 26, 2026
m-Chloroperbenzoic acid → N-{2-[4-(2-Methanesulfinyl-pyrimidin-4-ylethynyl)-phenyl]-1-methyl-ethyl}-acetamide
https://huagongshe.com/reaction/76179
Participants
| Role | Name | HCID | Charge |
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| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | N-{1-Methyl-2-[4-(2-methylsulfanyl-pyrimidin-4-ylethynyl)-phenyl]-ethyl}acetamide | HCID 66611369 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-{2-[4-(2-Methanesulfinyl-pyrimidin-4-ylethynyl)-phenyl]-1-methyl-ethyl}-acetamide | HCID 66614281 | — |
Reaction Steps
A mixture of 0.30 g (0.922 mmol) N-{1-methyl-2-[4-(2-methylsulfanyl-pyrimidin-4-ylethynyl)-phenyl]-ethyl}-acetamide (example 14.1) in 9 mL DCM is cooled down to 0° C. and charged with 0.27 g (1.10 mmol; 70% purity) 3-chloroperoxybenzoic acid. The mixture is stirred for 30 min at constant temperature. The mixture is poured onto sat. aq. NaHCO3 solution. The organic layer is separated, dried with Na2SO4 and filtered. The resulting mixture can be used directly used in the following reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08835472B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-edfcfc2ce2864381b67df2a46129db22 |
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| Source note | uspto-grants-2014_09 |
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