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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508415Generated: November 1, 2026

Formaldehyde → HCID 68503636, compound

https://huagongshe.com/reaction/1508415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium CarbonateHCID 10340—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 68500709HCID 68500709—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 68503636HCID 68503636—

Reaction Steps

To a solution of 2-(2-(2-(tert-butyldiphenylsilyloxy)ethyl)-5-(2,5-difluorophenyl)-2-phenyl-1,3,4-thiadiazol-3(2H)-yl)-4,5,6,7-tetrahydrothiazol[5,4-c]pyridine (0.157 g, 0.225 mmol) in 5 mL DCE was added formaldehyde (0.067 mL, 37 wt % in water, 0.901 mmol) followed by sodium triacetoxyborohydride (0.052 g, 0.248 mmol). The resulting suspension was stirred vigorously at room temperature overnight, then treated with saturated Na2CO3 solution (30 mL) and stirred for 10 minutes. The mixture was extracted with EtOAc (3×30 mL) and the combined organic phases were washed with brine (20 mL), dried over Na2SO4 and concentrated in vacuo. The residue was purified by flash column chromatography (0-1% MeOH/DCM) to afford the desired product as a bright yellow foam, 0.119 g, 74%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221841B2
Source datasetuspto-grants-2015_12
ORD IDord-55e55b435d2a43878dc717d2d8ef1828
Source noteuspto-grants-2015_12