HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809195Generated: October 25, 2026
N-bromobutanimide → 3-Bromo-8-chloro-6-methyl-imidazo[1,2-a]pyrazine
https://huagongshe.com/reaction/1809195
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 8-Chloro-6-methyl-imidazo[1,2-a]pyrazine | HCID 10374814 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Bromo-8-chloro-6-methyl-imidazo[1,2-a]pyrazine | HCID 58337100 | 97.3% |
Reaction Steps
N-bromosuccinimide (348 mg, 1.96 mmol) is added to a solution of 8-chloro-6-methyl-imidazo[1,2-a]pyrazine (337 mg, 2.02 mmol) in DCM (6.1 mL) and the reaction is stirred at 40° C. for 10 min and then at room temperature for 1 h 30 min. The reaction mixture is diluted with DCM and washed twice with 4 mL of Na2CO3 sat., dried with MgSO4 anh., filtered and concentrated in vacuo to give 3-bromo-8-chloro-6-methyl-imidazo[1,2-a]pyrazine as a yellow solid (470 mg, 95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08362018B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-226e866b4afc4301824e47118faf831a |
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| Source note | uspto-grants-2013_01 |
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