HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209027Generated: November 1, 2026
triethylorthoformate Acetic anhydride → 6-Bromo-4-chloro-3-methyl-imidazo[4,5-c]pyridine
https://huagongshe.com/reaction/2209027
Participants
| Role | Name | HCID | Charge |
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| Reactant | triethylorthoformate Acetic anhydride | HCID 88354608 | — |
| Reactant | 6-bromo-2-chloro-N3-methylpyridine-3,4-diamine | HCID 117842871 | — |
| Product | 6-Bromo-4-chloro-3-methyl-imidazo[4,5-c]pyridine | HCID 117843576 | — |
Reaction Steps
The above crude diamine 2.59-A was dissolved in a mixture of triethylorthoformate:Acetic anhydride (1:1, 9 mL). The reaction mixture was heated to 155° C. for 1 h, cooled to rt and then evaporated. The residue was dissolved in 2.5M NaOH (20 mL) and heated at 50° C. 45 min. The resulting solution was cooled to rt, neutralized with AcOH, and cooled to 0° C. The precipitate was filtered to give 6-bromo-4-chloro-3-methyl-3H-imidazo[4,5-c]pyridine 2.60.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09376441B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-3460ffc78e9541578b29b5d1822a96a1 |
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| Source note | uspto-grants-2016_06 |
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