HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241013Generated: October 30, 2026
Isobutyl chloroformate → isobutyl 6-bromo-2-methyl-1H-imidazo[4,5-b]pyridine-1-carboxylate
https://huagongshe.com/reaction/241013
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 6-bromo-2-methyl-1H-imidazo(4,5-b)pyridine | HCID 1958572 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | isobutyl 6-bromo-2-methyl-1H-imidazo[4,5-b]pyridine-1-carboxylate | HCID 66820076 | 46% |
Reaction Steps
To a solution of 6-bromo-2-methyl-1H-imidazo[4,5-b]pyridine (3.40 g, 16.0 mmol) and diisopropylethylamine (6.5 mL, 65 mmol) in N,N-dimethylformamide (20 mL) cooled in an ice bath was added dropwise isobutyl chloroformate (2.51 mL, 19.2 mmol) and the mixture was warmed to room temperature. After 1 hour the reaction was diluted with ethyl acetate (80 mL) and washed with water (60 mL), 10% aqueous citric acid (40 mL) and brine (20 mL). The organic phase was dried over anhydrous sodium sulfate, filtered and concentrated to a slurry. The residue was triturated diethyl ether (100 mL) and the solid isolated by filtration to give isobutyl 6-bromo-2-methyl-1H-imidazo[4,5-b]pyridine-1-carboxylate (2.3 g, 46% yield). MS (EI) for C12H14BrN3O2: 313 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08648066B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-2f4846d5d4d64fdcb3c7c8c86601ecab |
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| Source note | uspto-grants-2014_02 |
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