HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589804Generated: October 30, 2026
Stannous chloride dihydrate → HCID 61676010, compound
https://huagongshe.com/reaction/589804
Participants
| Role | Name | HCID | Charge |
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| Reactant | Stannous chloride dihydrate | HCID 61436 | — |
| Reactant | HCID 90450868 | HCID 90450868 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 61676010 | HCID 61676010 | 73% |
Reaction Steps
To a suspension of 6-bromo-2-(2-chloro-5-nitrophenyl)-1H-imidazo[4,5-b]pyridine I-2a (18 g, 50.91 mmol, 1.00 equiv) in ethanol (200 mL) was added SnCl2.2H2O (17.3 g, 76.55 mmol, 1.50 equiv) and heated to reflux overnight. The resulting mixture was concentrated under vacuum and the residue was diluted with 200 mL of H2O. The pH value of the mixture was adjusted to 8 with sodium carbonate (sat.). A filtration was performed and the solids were applied on a silica gel column and eluted with ethyl acetate/PE (1/1) to give 12 g (73%) of 3-[6-bromo-1H-imidazo[4,5-b]pyridin-2-yl]-4-chloroaniline (I-2b) as a yellow solid. 1H-NMR (DMSO, 400 MHz): 13.00-13.53 (m, 1H), 8.46 (s, 1H), 8.30 (brs, 1H), 7.26 (d, J=8.4 Hz, 1H), 7.05 (brs, 1H), 6.76 (dd, J=8.4, 2.8 Hz, 1H), 5.57 (brs, 2H). MS M/Z=325 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09233961B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-ee511a73c745436d8f97816350f222e2 |
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| Source note | uspto-grants-2016_01 |
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