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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2367758Generated: October 31, 2026

Triethylamine → HCID 178431605, compound

https://huagongshe.com/reaction/2367758

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,2-Dimethyl-1,3-dioxan-5-oneHCID 2733141—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-Cyano-1h-imidazole-2-carboxylic acid (2-cyclohex-1-enyl-4-piperidin-4-yl-phenyl)-amide trifluoroacetic acid saltHCID 178510383—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 178431605HCID 17843160528.1%

Reaction Steps

To a slurry of 4-cyano-1H-imidazole-2-carboxylic acid (2-cyclohex-1-enyl-4-piperidin-4-yl-phenyl)-amide trifluoroacetic acid salt (81 mg, 0.16 mmol, as prepared in Example 14, step (b)) in CH2Cl2 (3 mL) was added NEt3 (33 μL, 0.24 mmol). The solution was then treated with 2,2-dimethyl-[1,3]dioxan-5-one (31 mg, 0.24 mmol) and the reaction was allowed to stir for 3 h. At this time NaBH(OAc)3 (51 mg, 0.24 mmol) was added in one portion, and the reaction was allowed to stir for an additional 4 h. The reaction was diluted with H2O (10 mL) and extracted with EtOAc (2×25 mL). The organic extracts were dried (Na2SO4) and concentrated in vacuo. Purification by silica gel preparative thin layer chromatography (10% MeOH—CHCl3) afforded 22 mg (28%) of the title compound as an off-white semi-solid. Mass spectrum (ESI, m/z): Calcd. for C28H35N5O3, 490.2 (M+H). found 490.6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697716B2
Source datasetuspto-grants-2014_04
ORD IDord-a7fa6d1c77c04f6585582f5c46aa81bc
Source noteuspto-grants-2014_04