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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541441Generated: October 31, 2026

Acetic Acid → HCID 178424625, compound

https://huagongshe.com/reaction/541441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant3-OxetanoneHCID 15024254—
ReactantSodium cyanoborohydride [MI]HCID 20587905—
ReactantHCID 68288226HCID 68288226—
SolventDichloromethaneHCID 6344—
SolventMeOH tetrahydrofuranHCID 21899815—
ProductHCID 178424625HCID 17842462560%

Reaction Steps

A mixture of 4-(1-(2,4-dimethyl-5-(4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridin-2-yl)benzoyl)piperidin-4-yl)benzonitrile (compound 2.9, 62 mg), oxetan-3-one (18 μl), sodium cyanotrihydroborate (18 mg), and acetic acid (80 μl) in MeOH/THF (1:1 v/v) was stirred for 16 hours. The reaction was then diluted with dichloromethane, washed with saturated sodium bicarbonate solution followed by brine. The organic layer was dried (MgSO4) and concentrated. The residue was purified by preparative TLC at 8% MeOH in DCM to give 42 mg white solid (60%). m/z (ES+) 496 (M+H)+. 1H NMR (400 MHz, Chloroform-d) δ 7.63 (d, 2H), 7.32 (d, 2H), 7.27 and 7.20 (2 singlet, amide rotamers, 1H), 7.02 (s, 1H), 4.96 (s, 1H), 4.74 (m, 4H), 3.88-3.77 (m, 1H), 3.63 (d, 1H), 3.49 (d, 2H), 3.08 (t, 1H), 2.97-2.62 (m, 6H), 2.45 (d, 3H), 2.31 and 2.22 (2 singlets, amide rotamers, 3H), 2.11-1.40 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871790B2
Source datasetuspto-grants-2014_10
ORD IDord-b27a8ccc96174920ae62406c48a41459
Source noteuspto-grants-2014_10