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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1039705Generated: November 1, 2026

Formaldehyde → HCID 67270741, compound

https://huagongshe.com/reaction/1039705

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantTrimethyl orthoformateHCID 9005—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 57950902HCID 57950902—
SolventDichloromethaneHCID 6344—
ProductHCID 67270741HCID 67270741—

Reaction Steps

In a 15-mL RB flask, N-((1S,2R)-1-((3-bromo-4-fluorophenyl)methyl)-3-(((4′S)-6′-(2,2-dimethylpropyl)-3′,4′-dihydrospiro[cyclobutane-1,2′-pyrano[2,3-b]pyridin]-4′-yl)amino)-2-hydroxypropyl)acetamide (0.027 g, 0.048 mmol) was dissolved in DCM (1.5 mL). Trimethyl orthoformate (0.13 ml, 1.2 mmol) was added, followed by addition of Formaldehyde (37%, 0.0089 ml, 0.12 mmol) as an aqueous solution. The mixture was stirred at ambient temperature for 2 h. Then sodium triacetoxyborohydride (0.036 g, 0.17 mmol) was added, and the mixture was stirred at ambient temperature overnight. The reaction mixture was quenched with 10% aqueous sodium carbonate (5 mL), stirred vigorously for 2 h, and diluted with DCM (60 mL). The organic layer was separated and extracted with dilute brine (5 mL), dried over sodium sulfate and concentrated. The residue was purified by passing it through silica gel (20 g; deactivated with triethylamine (2.0 mL)), eluting with 95% EtOAc-hexane to provide the title compound. MS m/z 576/578 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08552181B2
Source datasetuspto-grants-2013_10
ORD IDord-dff0b5f7bf2949b5abcb1989836adada
Source noteuspto-grants-2013_10