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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117356Generated: October 30, 2026

Stannous chloride dihydrate → HCID 59815651, compound

https://huagongshe.com/reaction/2117356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannous chloride dihydrateHCID 61436—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 59815657HCID 59815657—
SolventEthanolHCID 702—
ProductHCID 59815651HCID 59815651—

Reaction Conditions

Temperature70 °C

Reaction Steps

N-[4-(benzyloxy)phenyl]-5-bromo-3-nitropyridin-2-amine (28.5 g, 0.071 mmol) and tin (II) chloride dihydrate (160.67 g, 0.712 mmol) were dissolved in 500 mL ethanol under N2 and the reaction mixture heated at reflux (70° C.) for 30 min. Sodium bicarbonate was then added to the cooled mixture until the pH was greater than 9.5, and then the mixture was filtered through celite which was washed with methanol. The combined organic phases were concentrated in vacuo before being re-constituted in CH2Cl2, drying over Na2SO4, and concentration in vacuo to yield N2-[4-(benzyloxy)phenyl]-5-bromopyridine-2,3-diamine. 1H NMR (400 MHz, CDCl3) δ 3.44 (bs, 2H), 5.07 (s, 2H), 6.02 (bs, 1H), 6.97 (dt, 2H, J=5.6, 3.6 Hz), 7.12 (d, 1H, J=2.0 Hz), 7.32 (dt, 2H, J=4.8, 0.4 Hz), 7.34-7.48 (m, 5H), 7.84 (d, 1H, J=2 Hz); MS (ES+): m/z 371[MH+], 372 (35) [MH2+]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442709B2
Source datasetuspto-grants-2008_10
ORD IDord-722db3feb1f5439d9964561e222c1af3
Source noteuspto-grants-2008_10