HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylamine → (7-Chlorothieno[3,2-b]pyridin-2-yl)(pyrrolidin-1-yl)methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | 7-Chloro-N,N-dimethylthieno[3,2-b]pyridine-2-carboxamide | HCID 22143537 | — |
| Product | (7-Chlorothieno[3,2-b]pyridin-2-yl)(pyrrolidin-1-yl)methanone | HCID 11173165 | — |
Reaction Steps
Following the procedures described above for the synthesis of compound 5 (scheme 1, example 1) but replacing dimethyl amine in the step 4 for pyrrolidine, title compound 139 was obtained. LRMS (M+1) 267.1 (100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07772247B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-be6a7d91d8b44742b1652ba84dfd3ae0 |
| Source note | uspto-grants-2010_08 |