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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 519095Generated: October 30, 2026

Sodium Thiosulfate → HCID 86727364, compound

https://huagongshe.com/reaction/519095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantSodium BicarbonateHCID 516892—
ReactantTetra-n-butylammonium tribromideHCID 23500184—
ReactantHCID 86727365HCID 86727365—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 86727364HCID 8672736457%

Reaction Steps

To a solution of 4-(4-methyl-3-oxo-2,3,4,10-tetrahydro-9-oxa-1,2,4a-triaza-phenanthren-6-yl)-piperidine-1-carboxylic acid tert-butyl ester (Example #71, Step B, 0.50 g, 1.249 mmol) in DCM (5 mL) and MeOH (5 mL) was added tetrabutylammonium tribromide (0.662 g, 1.373 mmol) portionwise and the reaction mixture was stirred for 30 min at ambient temperature. Saturated aqueous Na2S2O3 solution (5 mL) was added and the pH was adjusted to 7 by the addition of saturated aqueous NaHCO3 solution. The mixture was extracted with DCM (3×20 mL). The combined organic layers were washed with brine (20 mL), dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by column chromatography on silica gel (eluting with 20% EtOAc in petroleum ether) to give 4-(7-bromo-4-methyl-3-oxo-2,3,4,10-tetrahydro-9-oxa-1,2,4a-triaza-phenanthren-6-yl)-piperidine-1-carboxylic acid tert-butyl ester (0.34 g, 57%). LC/MS (Table 1, Method 2) Rt=1.289 min.; MS m/z: 479/481 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115151B2
Source datasetuspto-grants-2015_08
ORD IDord-65d5686b2a1c4760b4b65f48c4cdcd79
Source noteuspto-grants-2015_08