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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2200898Generated: October 30, 2026

Formaldehyde → HCID 73214394, compound

https://huagongshe.com/reaction/2200898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 118158105HCID 118158105—
SolventMethanolHCID 887—
ProductHCID 73214394HCID 7321439427.4%

Reaction Steps

In methanol (50 mL) was dissolved the above N-(7-azaspiro[3.5]nonan-2-ylmethyl)-2-(3-azabicyclo[3.1.0]hexan-3-yl)-4-((3-chloro-4-methoxybenzyl)amino)pyrimidine-5-formamide (357 mg, 0.7 mmol). Formalin (284 mg, 3.5 mmol) was added. Sodium borohydride (133 mg, 3.5 mmol) was added slowly. The reaction was continued for 10 h then quenched with water. The reaction mixture was extracted with ethyl acetate. The organic phase was dried and concentrated. The obtained solid was purified by silica gel column chromatography (DCM/methanol=20/1) to give 2-(3-azabicyclo[3.1.0]hexan-3-yl)-4-((3-chloro-4-methoxybenzyl)amino)-N-((7-methyl-7-azaspiro[3.5]nonan-2-yl)methyl)pyrimidine-5-form amide (100 mg, 27.4% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359371B2
Source datasetuspto-grants-2016_06
ORD IDord-995df5322fc749bd9b50c4201133fd6a
Source noteuspto-grants-2016_06