HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1454993Generated: October 31, 2026
Potassium Carbonate → HCID 67307138, compound
https://huagongshe.com/reaction/1454993
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3-(3-Bromophenyl)propan-1-ol | HCID 18785928 | — |
| Reactant | HCID 60209555 | HCID 60209555 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67307138 | HCID 67307138 | 39.3% |
Reaction Steps
A solution of 1.57 g (6.7 mmol) of 3-(3-bromophenyl)propan-1-ol, prepared in step 7.1., and 1.73 ml (10.1 mmol) of diisopropylethylamine in 38 ml of dichloromethane, cooled to 0° C., is admixed with 0.63 ml (8.14 mmol) of methanesulphonyl chloride. Stirring is continued in the cold for 0.5 hour and then at ambient temperature for 2 hours. The mixture is concentrated under reduced pressure and then the residue is suspended in 35 ml of acetonitrile. 1.34 g (5.35 mmol) of 2-(methylamino)-2-oxoethyl piperazine-1-carboxylate hydrochloride, prepared in accordance with Example 3.3., and 2.2 g (16 mmol) of potassium carbonate are added. The mixture is heated at 75° C. for 16 hours. After cooling to ambient temperature it is concentrated under reduced pressure and then the residue is taken up in water. It is extracted with ethyl acetate and dried over sodium sulphate. Following filtration, the organic phase is concentrated under reduced pressure. It is purified by chromatography on silica gel, eluting with a 98/2 mixture of dichloromethane and methanol. Crystallization from diisopropyl ether gives 0.84 g (2.10 mmol) of white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07482346B2 |
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| Source dataset | uspto-grants-2009_01 |
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| ORD ID | ord-5aa8e18711e44008b5bf923148ad37bb |
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| Source note | uspto-grants-2009_01 |
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