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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571397Generated: October 30, 2026

Sodium Thiosulfate → HCID 71554947, compound

https://huagongshe.com/reaction/571397

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 71555390HCID 71555390—
SolventAcetonitrileHCID 6342—
ProductHCID 71554947HCID 7155494743%

Reaction Steps

To a stirred solution of 1-[(1R)-1-(4-chlorophenyl)ethyl]-3-[3-(2-methylpyridin-4-yl)-1H-pyrazolo[4,3-c]pyridin-6-yl]urea (Example 19; 82 mg, 0.202 mmol) in MeCN (2 mL) was added NBS (47 mg, 0.262 mmol). The mixture was left to stir for 1 h at room temperature and then treated with 1N Na2S2O3, and extracted with chloroform:iPrOH (3:1, x3). The combined organics were dried (Na2SO4), concentrated in vacuo and purified by column chromatography on silica gel to yield 1-[7-bromo-3-(2-methylpyridin-4-yl)-1H-pyrazolo[4,3-c]pyridin-6-yl]-3-[(1R)-1-(4-chlorophenyl)ethyl]urea (42 mg, 0.086 mmol, 43%). MS ESI calc'd. for C21H19BrClN6O [M+1]+ 485, found 485.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09023865B2
Source datasetuspto-grants-2015_05
ORD IDord-372e81abda3f4fbd9c50bbb68038b2f8
Source noteuspto-grants-2015_05