Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2208933Generated: October 30, 2026

Sodium borohydride → HCID 70874001, compound

https://huagongshe.com/reaction/2208933

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 70874027HCID 70874027—
SolventMethanolHCID 887—
ProductHCID 70874001HCID 70874001—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 5-chloro-N-((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-3-(ethyl(4-oxocyclohexyl)amino)-2-methylbenzamide (0.30 g, 0.68 mmol) in MeOH was added NaBH4 (0.038 g, 1.01 mmol) slowly at 0° C. The resulting reaction mixture was stirred at 0° C. for 2 h. On completion, the reaction was quenched with water and extracted with ethyl acetate. The combined organic layers were washed with water, dried, concentrated under reduced pressure and the crude material obtained was purified by acetonitrile and ether washings to afford the title compound as a mixture of isomers (175 mg, 58%). LCMS: 446.35 (M+1)+; HPLC: 74.32% & 24.18% (@ 210-370 nm) (Rt; 5.157 & 5.276); Method: Column: YMC ODS-A 150 mm×4.6 mm×5μ; Mobile Phase: A; 0.05% TFA in water/B; 0.05% TFA in acetonitrile; Inj. Vol: 10 μL, Col. Temp.: 30° C.; Flow rate: 1.4 mL/min.; Gradient: 5% B to 95% B in 8 min, Hold for 1.5 min, 9.51-12 min 5% B); 1H NMR (DMSO-d6, 400 MHz) δ 11.49 (s, 1H), 8.25 (s, 1H), 7.17 (s, 1H), 6.96 (s, 1H), 5.86 (s, 1H), 4.25 (d, 2H, J=4 Hz), 3.33 (m, 1H), 3.04 (m, 2H), 2.19 (s, 3H), 2.14 (s, 3H), 2.10 (s, 3H), 1.78 (m, 2H), 1.66 (m, 2H), 1.38 (m, 3H), 1.10 (m, 2H), 0.78 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376422B2
Source datasetuspto-grants-2016_06
ORD IDord-2147e599ab984a6ead580a85f6917f11
Source noteuspto-grants-2016_06