HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 564987Generated: October 26, 2026
Chloroacetamide → Methyl 7-carbamoylmethoxy-1-methyl-2-indolecarboxylate
https://huagongshe.com/reaction/564987
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetamide | HCID 6580 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl 7-hydroxy-1-methyl-2-indolecarboxylate | HCID 21194122 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 7-carbamoylmethoxy-1-methyl-2-indolecarboxylate | HCID 21194580 | 84.4% |
Reaction Steps
After 0.50 g (2.44 mmol) of methyl 7-hydroxy-1-methyl-2-indolecarboxylate was added to a suspension of 0.01 g (2.44 mmol) of 60% sodium hydride in 25 ml of dimethyl-formamide, the mixture was stirred at room temperature until the mixture became a transparent solution. Then 0.25 g (2.68 mmols) of 2-chloroacetamide was added dropwise to the transparent solution at room temperature followed by stirring at 50° C. for an hour. The reaction mixture was poured onto ice water. The resulting mixture was then extracted three times with ethyl acetate. The combined extracts were washed with water. After drying over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography to give 0.54 g (84.4%) of methyl 7-carbamoylmethoxy-1-methyl-2-indolecarboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06169107A |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-bb91b637e931465c970104e95c24bc0e |
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| Source note | uspto-grants-2001_01 |
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