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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666155Generated: October 31, 2026

Acetic Acid → HCID 57911418, compound

https://huagongshe.com/reaction/1666155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantFormaldehydeHCID 712—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 57911461HCID 57911461—
SolventAcetonitrileHCID 6342—
ProductHCID 57911418HCID 5791141840.9%

Reaction Steps

SODIUM CYANOBOROHYDRIDE (108 mg, 1.721 mmol) was added to the Acetonitrile (2 mL) solution of (6R,9R)-2-amino-6-(2,3-difluorophenyl)-6,7,8,9-tetrahydro-5H-cyclohepta[b]pyridin-9-yl 4-(2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-1-yl)piperidine-1-carboxylate (46 mg, 0.086 mmol) and FORMALDEHYDE (1 mL, 13.43 mmol) at rt. The reaction was stirred at room temperature for 4 hours. ACETIC ACID (0.5 mL, 8.73 mmol) was added to the reaction mixture and the reaction was stirred overnight. Volatile was removed mostly via vacuum and the crude was added NaOH (1N) and stirred at room temperature for 1 hour before extract with ethyl acetate. The ethyl acetate layer was dried (Na2SO4), filtered and concentrated. Flash column by methanol in CH2Cl2 from 0 to 4% to 8% gave the desired product (19.8 mg, 39%). MS(ESI)[M+H+]=563.42.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044043B2
Source datasetuspto-grants-2011_10
ORD IDord-62e23a7e568b4ccbb16002ab977e3f7f
Source noteuspto-grants-2011_10