HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → Ethyl 7-benzyloxy-4-chloro-1-methyl-2-indolecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 7-benzyloxy-4-chloro-2-indolecarboxylate | HCID 21194186 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 7-benzyloxy-4-chloro-1-methyl-2-indolecarboxylate | HCID 21194304 | — |
Reaction Steps
The reaction was carried out in a manner similar to Reference Example 18 a) except for using 8.00 g (24.3 mmol) of ethyl 7-benzyloxy-4-chloro-2-indolecarboxylate, 0.97 g (24.3 mmol) of 60% sodium hydride, 10.3 g (72.8 mmol) of methyl iodide and 200 ml of dimethylformamide. Ethyl 7-benzyloxy-4-chloro-1-methyl-2-indolecarboxylate was thus obtained in the yield of 7.71 g (92.4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06169107A |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-bbda29043f72492082da87ff3f93c0b0 |
| Source note | uspto-grants-2001_01 |