HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374024Generated: October 31, 2026
Dimethyl Sulfate → HCID 6481889, compound
https://huagongshe.com/reaction/374024
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 19808758 | HCID 19808758 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 6481889 | HCID 6481889 | 51.3% |
Reaction Steps
In 10 ml of N,N-dimethylformamide was dissolved 380 mg of N-(2-dimethylaminoethyl)-6-methoxycarbazole-3,4-dicarboximide. Thereto was added 45 mg of 60% sodium hydride. The mixture was stirred at 40° C. for 20 minutes and then cooled to 20° C. Thereto was added 140 mg of dimethyl sulfate, and the resulting mixture was stirred at the same temperature for 2 hours. The solvent was removed by distillation under reduced pressure. The residue was mixed with 50 ml of ethyl acetate and 25 ml of water to dissolve the residue. The organic layer was separated, washed with an aqueous saturated sodium chloride solution, and dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure. The residue was recrystallized from n-propanol to obtain 200 mg (yield: 50%) of N-(2-dimethylaminoethyl)-6-methoxy-9-methylcarbazole-3,4-dicarboximide as yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05166204 |
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| Source dataset | uspto-grants-1992_11 |
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| ORD ID | ord-c2e3c9c7a269429eb1529fb8b5111bc3 |
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| Source note | uspto-grants-1992_11 |
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