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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 519240Generated: October 30, 2026

Sodium Thiosulfate → HCID 86727639, compound

https://huagongshe.com/reaction/519240

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantSodium BicarbonateHCID 516892—
ReactantTetra-n-butylammonium tribromideHCID 23500184—
ReactantHCID 86727640HCID 86727640—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 86727639HCID 8672763981%

Reaction Conditions

Temperature20 °C

Reaction Steps

To a mixture of (R)-6-[(1,3-dimethyl-azetidin-3-yl)-methyl-amino]-4-methyl-2,10-dihydro-9-oxa-1,2,4a-triaza-phenanthren-3-one (3 g, 9.11 mmol) in DCM (40 mL) and MeOH (20 mL) was added tetra-n-butylammonium tribromide (6.59 g, 13.66 mmol) in portions and the reaction mixture was stirred at 20° C. for 16 h. Saturated aqueous Na2S2O3 (10 mL) was added and saturated aqueous sodium bicarbonate (5 mL) was added to neutralize the mixture. The organic phase was separated, dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by column chromatography on basified silica gel (eluting with 10% MeOH in DCM) to give (R)-7-bromo-6-[(1,3-dimethyl-azetidin-3-yl)-methyl-amino]-4-methyl-2,10-dihydro-9-oxa-1,2,4a-triaza-phenanthren-3-one (3 g, 81%) as a brown solid. LC/MS (Table 1, Method 3), Rt=1.060 min.; MS m/z: 410 [M+H+2]+& 408 [M+H]+. SFC (Table 1, Method 49), Rt=5.174 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115151B2
Source datasetuspto-grants-2015_08
ORD IDord-8c9274b496334898be8cab8d1055aa85
Source noteuspto-grants-2015_08