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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 511607Generated: October 28, 2026

Acetic Acid → HCID 178491013, compound

https://huagongshe.com/reaction/511607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantFormaldehydeHCID 712—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 178491006HCID 178491006—
SolventMethanolHCID 887—
ProductHCID 178491013HCID 17849101380.7%

Reaction Steps

A solution of 7-((3aS,4R,6R,6aR)-6-(((3-(2-(6-chloro-5-(trifluoromethyl)-1H-benzo[d]imidazol-2-yl)ethyl)cyclobutyl)amino)methyl)-2,2-dimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-yl)-N-(2,4-dimethoxybenzyl)-7H-pyrrolo[2,3-d]pyrimidin-4-amine (76 mg, 0.10 mmol) in methanol (2.5 mL) was treated with sodium cyanoborohydride (84 mg, 1.3 mmol). The pH of the solution was adjusted to ˜6 by the dropwise addition of a 10% (v/v) solution of glacial acetic acid in methanol. The mixture was treated with 37% aqueous formaldehyde (0.12 mL, 1.7 mmol) dropwise and the mixture was stirred at room temperature till complete by LCMS. After 2 h, the reaction was complete and the reaction mixture was concentrated to remove the methanol. The aqueous solution that remained was diluted with 7 mL NaHCO3 and the aqueous phase was extracted with three 10 mL portions of CH2Cl2. The organic phase was dried over Na2SO4, filtered, and concentrated to yield a colorless stiff foam/glass. The crude material was purified by flash chromatography (20 g silica gel; 4% 7N NH3 in CH3OH/CH2Cl2) to yield the title compound (62 mg, 80%) as a colorless glass: MS (ESI+) for C39H45ClF3N7O4 m/z 768.0 (M+H)+; MS (ESI−) for C39H45ClF3N7O4 m/z 766.3 (M−H)−; HPLC purity 92.1% (ret. time, 3.29 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096634B2
Source datasetuspto-grants-2015_08
ORD IDord-c3eb48d438d94b2da20ccfdbc4bc77e8
Source noteuspto-grants-2015_08