Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine chloride | HCID 24640 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Sodium Pyrosulfite | HCID 656671 | — |
| Reactant | 6-Bromo-9H-pyrrolo[2,3-b:5,4-c′]dipyridine | HCID 58266727 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 58266297 | HCID 58266297 | 84.2% |
Reaction Steps
A solution of iodine monochloride (32.5 g, 200 mmol) in acetic acid (120 mL) was added portionwise over 2 h to a mixture of 6-bromo-9H-dipyrido[2,3-b;4′,3′-d]pyrrole (5.0 g, 20 mmol) and sodium acetate (18.2 g, 221 mmol) in acetic acid (120 mL) at 100° C. The reaction mixture was cooled to ambient temperature and poured into saturated sodium metabisulfite solution (20% w/w, 400 mL). The resultant precipitate was collected by filtration and the solid was washed with water (50 mL) and diethyl ether (2×50 mL) then dried at 45° C. until constant weight was achieved, to afford the title compound as a grey solid (6.3 g, 83%). 1H NMR (DMSO-D6, 300 MHz): 12.49 (s, 1H), 9.14 (d, J=2.1 Hz, 1H), 8.79 (d, J=2.1 Hz, 1H), 8.71 (s, 1H), 8.49 (s, 1H). LCMS (Method B): RT=3.40 min, M+H+=374/376.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09216980B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-746b7f06e4e54f408bf32b3d2f76f5c4 |
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| Source note | uspto-grants-2015_12 |
|---|