HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Bromo-1,1,1-triethoxypentane → 6-Benzyloxy-5-(5-ethoxycarbonylpentyl)-imidazo[1,5-a]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Bromo-1,1,1-triethoxypentane | HCID 13206137 | — |
| Reactant | 6-Benzyloxy-5-methylimidazo[1,5-a]pyridine | HCID 13373636 | — |
| Product | 6-Benzyloxy-5-(5-ethoxycarbonylpentyl)-imidazo[1,5-a]pyridine | HCID 20446659 | — |
Reaction Steps
The condensation of 6-benzyloxy-5-methylimidazo[1,5-a]pyridine with 5-bromo-1,1,1-triethoxypentane essentially by the procedure described in Example 1 yields 6-benzyloxy-5-(5-ethoxycarbonylpentyl)-imidazo[1,5-a]pyridine; NMR (CDCl3) 1.4 (3H), 4.17 (2H), 4.97 (2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04470986 |
| Source dataset | uspto-grants-1984_09 |
| ORD ID | ord-8b66938fc2a643659ca0daf8aa3d323e |
| Source note | uspto-grants-1984_09 |