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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1055004Generated: October 31, 2026

Sodium Bicarbonate → HCID 90017711, compound

https://huagongshe.com/reaction/1055004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl N-(triethylammoniosulfonyl)carbamateHCID 2724994—
ReactantHCID 90017038HCID 90017038—
SolventTetrahydrofuranHCID 8028—
ProductHCID 90017711HCID 90017711128.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

N′-(5-Ethyl-2-methylpyrimidin-4-yl)-3-(1-methyl-3-(pyrrolidin-1-yl)-1H-1,2,4-triazol-5-yl)propanehydrazide (56.6 mg, 158 μmol) in tetrahydrofuran (4 ml) was added to Burgess reagent (155 mg, 632 μmol). The mixture was heated in a sealed tube at 80° C. for 1 h. Saturated sodium bicarbonate solution was added and extracted with dichloromethane. The organic layers were dried over sodium sulfate and concentrated to an oil to afford the desired product (69 mg) as a yellow solid which was used without further purification in the next step. MS: m/z=341.2 (M+H+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394311B2
Source datasetuspto-grants-2016_07
ORD IDord-922df7ab2a5d4cf6bd9ed24684fec3b8
Source noteuspto-grants-2016_07