Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1778916Generated: November 4, 2026

Sodium triacetoxyborohydride → HCID 89498080, compound

https://huagongshe.com/reaction/1778916

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantThiomorpholine 1,1-dioxideHCID 6484228—
ReactantHCID 89498148HCID 89498148—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acidHCID 6422—
SolventEthyl AcetateHCID 8857—
ProductHCID 89498080HCID 89498080—

Reaction Steps

To a solution of EXAMPLE 167F (72 mg) and thiomorpholine 1,1-dioxide (13.5 mg) in dichloromethane (3 mL) was added sodium triacetoxyborohydride (32 mg). The mixture was stirred overnight. The mixture was dissolved in ethyl acetate (200 mL) and washed with 2N aqueous NaOH and brine, and dried over Na2SO4. Filtration and evaporation of the solvent gave crude product which was dissolved in dichloromethane (2 mL) and TFA (2 mL). After stirring overnight, the solvent was evaporated. The residue was purified by reverse phase chromatography using a Gilson system, eluting with 20-80% acetonitrile in 0.1% TFA water solution to provide the title compound. 1H NMR (300 MHz, dimethylsulfoxide-d6) δ ppm 12.86 (s, 1H), 8.04 (d, 1H), 7.79 (d, 1H), 7.62 (d, 1H), 7.42 (m, 5H), 6.97 (d, 1H), 4.96 (s, 2H), 4.10 (s, 3H), 3.53 (m, 8H), 3.02 (t, 2H), 2.13 (s, 3H), 1.43 (m, 10H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266877B2
Source datasetuspto-grants-2016_02
ORD IDord-8d6fdf5b9917472889022d3895c22f97
Source noteuspto-grants-2016_02