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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655308Generated: October 30, 2026

Formaldehyde → HCID 59320386, compound

https://huagongshe.com/reaction/655308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 59320197HCID 59320197—
SolventDichloromethaneHCID 6344—
ProductHCID 59320386HCID 5932038635%

Reaction Steps

To 3-(1-azetidin-3-yl-1H-pyrazol-4-yl)-6-(6-methyl-[1,2,4]triazolo[4,3-b]pyridazin-3-ylmethyl)-quinoline (194 mg, 0.4898 mmol) in dichloromethane (9 mL) was added formaldehyde (37% in water, 1.959 mmol, 147 uL). The solution was stirred at room temperature for 15 minutes and then sodium triacetoxyborohydride (260 mg, 1.22 mmol) was added. After 1 hour the solution was diluted with dichloromethane (6 mL) and washed with sodium bicarbonate (6 mL). The aqueous layer was extracted further with dichloromethane (6 mL). The combined dichloromethane layers were washed with brine (12 mL) and dried over Na2SO4. The filtrate was concentrated in vacuo onto silica gel and purified by flash chromatography (SiO2, CH2Cl2:CH3OH:NH4OH, 95:4.995:0.005-80:19.98:0.02) to return the title compound (69 mg, 35% yield). Analytical data presented in Table 2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071581B2
Source datasetuspto-grants-2011_12
ORD IDord-c14f9a67498e4aa7bbcfa5e0f81244f4
Source noteuspto-grants-2011_12