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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181411Generated: November 4, 2026

Formaldehyde → HCID 10390073, compound

https://huagongshe.com/reaction/2181411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 21354520HCID 21354520—
SolventMethanolHCID 887—
ProductHCID 10390073HCID 10390073106.8%

Reaction Steps

4-(4-Fluorophenyl)-2-(4-piperidinyl)-5-(2-(1-(S)-phenylethyl)amino-4-pyridinyl)thiazole (500 mg 1.09 mmol) is dissolved in MeOH (11 ml) and treated with an aqueous 36%-solution of formaldehyde (0.17 ml 2.18 mmol) and NaBH4 (83 mg 2.18 mmol), which is added as a solid in 3 portions. After 30 min at room temperature the reaction mixture is poured on water and extracted three times with ethyl acetate. The combined organic phases are dried over Na2SO4, filtered, evaporated to dryness and purified by SiO2 chromatography (tert.butyl methyl ether/MeOH/NH3conc. 95/4.5/0.5) to yield the title compound (550 mg 86%) as pale yellow foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06891039B2
Source datasetuspto-grants-2005_05
ORD IDord-c1f5f4aa1cb5495b81ca34351c568861
Source noteuspto-grants-2005_05