HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-dimethyl-1H-indole-2-carbaldehyde → 3-(methylaminomethyl)-1,2,7-trimethyl-1H-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-dimethyl-1H-indole-2-carbaldehyde | HCID 2771468 | — |
| Reactant | 1,2,7-trimethyl-1H-indole-3-carboxaldehyde | HCID 17604458 | — |
| Reactant | Methyl 2-((5-bromopyridin-2-yl)amino)acetate | HCID 22139049 | — |
| Product | 3-(methylaminomethyl)-1,2,7-trimethyl-1H-indole | HCID 11009005 | 71% |
Reaction Steps
According to the procedure of Preparation 13 (c) except substituting 1,2,7-trimethyl-1H-indole-3-carboxaldehyde for the 1,3-dimethyl-1H-indole-2-carboxaldehyde, the title compound (570 mg, 71%) was obtained as an oil which slowly crystallized: MS (ES) m/e 405.4 (2M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07879872B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-9f04972190e44dce8ab6675076b7171f |
| Source note | uspto-grants-2011_02 |