HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376879Generated: October 30, 2026
Dimethyl Sulfate → HCID 19360266, compound
https://huagongshe.com/reaction/376879
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 19360159 | HCID 19360159 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 19360266 | HCID 19360266 | 167.6% |
Reaction Steps
6-Chloro-3-(4-pyridinylamino)benzo[b]thiophene (3 g, 11.5 mmol) was added portionwise as a powder to an ice-cooled suspension of sodium hydride (60% oil dispersion, 0.7 g, 17.5 mmol, washed with heptane) in 25 mL of dimethylformamide. After anion formation was completed dimethyl sulfate (1.6 g, 12.7 mmol) was added. After one hour the reaction mixture was poured into ice-water and extracted with ether. The organic extract was washed with water and saturated sodium chloride solution, and dried (arhydrous magnesium sulfate), filtered and concentrated to give 3 g of a brown oil. Elution through silica with 10% methanol in ethyl acetate via flash column chromatography yielded 1.7 g of an amber oil. Conversion to the hydrochloride salt in 10% methanol in ether afforded 1.4 g of yellow crystals, mp 280-281° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06022880 |
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| Source dataset | uspto-grants-2000_02 |
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| ORD ID | ord-6bae1bbdd64e4e8a8e9cd9e9ece99601 |
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| Source note | uspto-grants-2000_02 |
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