HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 331010Generated: October 30, 2026
N-Iodosuccinimide → 4-bromo-3-iodo-2-methyl-1H-pyrrolo[2,3-b]pyridine
https://huagongshe.com/reaction/331010
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | 4-Bromo-2-methyl-1H-pyrrolo(2,3-b)pyridine | HCID 52987786 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-bromo-3-iodo-2-methyl-1H-pyrrolo[2,3-b]pyridine | HCID 71090193 | 93% |
Reaction Steps
To a mixture of 4-bromo-2-methyl-1H-pyrrolo[2,3-b]pyridine (D24) (1.65 g, 7.82 mmol) in DCM (70 mL) was added NIS (1.935 g, 8.60 mmol) at 0° C. and the mixture was stirred for 1.5 hour at 0° C. The mixture was evaporated in vacuo. DCM (ca. 20 mL) was added to the residue. The formed precipitate was filtered, rinsed with DCM to give the title compound (2.45 g). LCMS (A): m/z (M+H)+ 337/339, C8H6BrIN2 requires 336/338 (acidic).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08877742B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-864ac5436dfa4d54a94e5208c668edf3 |
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| Source note | uspto-grants-2014_11 |
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