HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methylindole-2-carboxaldehyde → 3,4-Dimethyl-2-(methylaminomethyl)thieno[2,3-b]thiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methylindole-2-carboxaldehyde | HCID 267164 | — |
| Reactant | 3,4-Dimethylthieno[2,3-B]Thiophene-2-Carbaldehyde | HCID 2778771 | — |
| Product | 3,4-Dimethyl-2-(methylaminomethyl)thieno[2,3-b]thiophene | HCID 22593756 | 53% |
Reaction Steps
According to the procedure of Preparation 24 (a), except substituting 3,4-dimethylthieno[2,3-b]thiophene-2-carboxaldehyde (0.5 g, 2.5 mmole) for the 1-methylindole-2-carboxaldehyde, the title compound (0.28 g, 53%) was prepared as a colorless oil: MS (ES) m/e 212 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08173646B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-5e55740b78644ed5827c445838b70bdb |
| Source note | uspto-grants-2012_05 |