HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-(Benzyloxy)-3-p-tolyl-3H-imidazo[4,5-b]pyridine → HCID 178426251, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-(Benzyloxy)-3-p-tolyl-3H-imidazo[4,5-b]pyridine | HCID 67311860 | — |
| Reactant | 5-(benzyloxy)-1-p-tolyl-1H-imidazo[4,5-b]pyridine | HCID 67313933 | — |
| Product | HCID 178426251 | HCID 178426251 | — |
Reaction Steps
From the mixture of 5-(benzyloxy)-3-p-tolyl-3H-imidazo[4,5-b]pyridine and 5-(benzyloxy)-1-p-tolyl-1H-imidazo[4,5-b]pyridine, the benzyl group was removed as described in Example 1.11, Step B. Purification by preparative HPLC gave the title compound as a white solid. 1H NMR (400 MHz, methanol-d4) δ ppm 2.41 (s, 3H), 6.70 (d, J=8.8 Hz, 1H), 7.36 (d, J=8.3 Hz, 2H), 7.67 (d, J=8.3 Hz, 2H), 7.95 (d, J=8.6 Hz, 1H), 8.43 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08507473B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-d0ffba72346248c3b5d8840be12ad88b |
| Source note | uspto-grants-2013_08 |