HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → ethyl 7-amino-4-chloro-1-(methoxymethyl)-1H-indole-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | ethyl 7-amino-1-(methoxymethyl)-1H-indole-2-carboxylate | HCID 57475944 | — |
| Solvent | Water | HCID 962 | — |
| Product | ethyl 7-amino-4-chloro-1-(methoxymethyl)-1H-indole-2-carboxylate | HCID 57476018 | 25.1% |
Reaction Steps
A mixture of ethyl 7-amino-1-(methoxymethyl)-1H-indole-2-carboxylate (3.18 g), N-chlorosuccinimide (1.74 g) and N,N-dimethylformamide (20 ml) was stirred overnight at room temperature. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4), and concentrated. The residue was subjected to silica gel column chromatography to give the title compound (0.91 g, yield 25%) as a yellow oil from a fraction eluted with ethyl acetate-hexane (1:4, volume ratio).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07777047B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-7270b02e628f495d8139488d0960dc15 |
| Source note | uspto-grants-2010_08 |