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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 564584Generated: October 29, 2026

Acetic Acid → HCID 57813303, compound

https://huagongshe.com/reaction/564584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactantrel-(2R,6S)-2,6-dimethylpiperazineHCID 6950261—
ReactantHCID 57813304HCID 57813304—
SolventDichloromethaneHCID 6344—
ProductHCID 57813303HCID 57813303—

Reaction Steps

N-{[1,6-Diethyl-4-(tetrahydro-2H-pyran-4-ylamino)-1H-pyrazolo[3,4-b]pyridin-5-yl]methyl}-N′-[(3′-formyl-6-methyl-3-biphenylyl)methyl]-1,3-benzenedicarboxamide (0.033 g, 0.05 mmol), (2R,6S)-2,6-dimethylpiperazine (0.00685 g, 0.06 mmol), and acetic acid (0.0036 g, 0.06 mmol) were combined in CH2Cl2 (2 mL). Sodium triacetoxyborohydride (0.0148 g, 0.07 mmol) was added and the mixture stirred overnight at room temperature. Solvents were concentrated, and the residue taken up in EtOAc, washed with 1N NaOH, brine, dried over anhydrous Na2SO4, filtered, and concentrated to give the crude product. The product was purified using a Gilson HPLC with a TFA system. The purified compound was taken up in EtOAc, washed 3× with 2.5 N NaOH, 1× with brine, dried over anhydrous Na2SO4, filtered, and concentrated to afford the title compound as a white solid. LC-MS m/z 757.2 (M+H)+, 1.37 min (ret time); mp 109-112° C. Analytical HPLC shows 99.8% purity, (ret time 10.205 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08067408B2
Source datasetuspto-grants-2011_11
ORD IDord-14810274fa8b46219ad387a9973f5979
Source noteuspto-grants-2011_11