HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(6-Chloro-3-nitropyridin-2-yl)-1,2,3,4-tetrahydroisoquinoline → 2-(5-chloro-2-methyl-1H-pyrrolo[2,3-c]pyridin-7-yl)-1,2,3,4-tetrahydro-isoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(6-Chloro-3-nitropyridin-2-yl)-1,2,3,4-tetrahydroisoquinoline | HCID 43152677 | — |
| Reactant | HCID 178456138 | HCID 178456138 | — |
| Product | 2-(5-chloro-2-methyl-1H-pyrrolo[2,3-c]pyridin-7-yl)-1,2,3,4-tetrahydro-isoquinoline | HCID 86615276 | — |
Reaction Steps
In accordance with the same procedures as in Step 3 of Example 642, except for using 2-(6-chloro-3-nitropyridin-2-yl)-1,2,3,4-tetrahydroisoquinoline prepared in Preparation 7 and isopropenylmagnesium bromide, the titled compound was obtained as yellow oil. (Yield: 35%) The product was used in the subsequent step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07662832B2 |
| Source dataset | uspto-grants-2010_02 |
| ORD ID | ord-54bb5fa3e7994a6bb1a1c501b8984102 |
| Source note | uspto-grants-2010_02 |