HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methyl-1H-indole-3-carbaldehyde → 2-chloro-1-methyl-2-(methylaminomethyl)-1H-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methyl-1H-indole-3-carbaldehyde | HCID 87894 | — |
| Reactant | 2-Chloro-1-methyl-1H-indole-3-carbaldehyde | HCID 314792 | — |
| Product | 2-chloro-1-methyl-2-(methylaminomethyl)-1H-indole | HCID 66905063 | 90% |
Reaction Steps
According to the procedure of Preparation 12, except substituting 2-chloro-1-methyl-1H-indole-3-carboxaldehyde (3.0 g, 15.5 mmole) for the 1-methylindole-3-carboxaldehyde, the title compound (2.91 g, 90%) was prepared as an oil: 1H NMR (400 MHz, CDCl3) δ 7.60 (d, J=7.9 Hz, 1H), 7.22 (m, 2H), 7.13 (m, 1H), 3.92 (s, 2H), 3.71 (s, 3H), 2.44 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07250424B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-d3cdaba652b9471b8c7e90818dd723a5 |
| Source note | uspto-grants-2007_07 |