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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 914021Generated: October 29, 2026

Formaldehyde → HCID 25160582, compound

https://huagongshe.com/reaction/914021

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 57546242HCID 57546242—
CatalystAcetic AcidHCID 176—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 25160582HCID 25160582—

Reaction Steps

(±)-tert-Butyl 4-((1-(1-(cyclopropylmethyl)-5-methyl-1H-indazol-7-yl)ethoxy)methyl)-4-(4-fluorophenyl)piperidine-1-carboxylate (7 mg, 0.01 mmol) was dissolved in trifluoroacetic acid (50% in dichloromethane, 1 mL) and stirred at room temperature for 1 h. The reaction was concentrated, loaded onto a strong cation exchange cartridge in methanol, and flushed with several volumes of methanol which were discarded. The crude secondary amine was eluted in 2 M ammonia in methanol and concentrated. The resulting residue was dissolved in acetonitrile (1 mL), cooled to 0° C., and treated with sodium cyanoborohydride (4.2 mg, 0.07 mmol) and formalin (37 μL). After 5 min, the reaction was treated with a few drops of acetic acid. The ice bath was removed and stirring continued for 1 h. The reaction was concentrated and purified by flash chromatography on silica gel (10% methanolic ammonia/methylene chloride) to afford 4 mg (68%). LC/MS (HPLC method 1): tR=2.49 min, 436.59(MH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08026257B2
Source datasetuspto-grants-2011_09
ORD IDord-b32d400a24004e72bc132008eba7d816
Source noteuspto-grants-2011_09