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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748390Generated: November 1, 2026

Dimethyl Sulfide → HCID 86301484, compound

https://huagongshe.com/reaction/1748390

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfideHCID 1068—
ReactantSodium BicarbonateHCID 516892—
Reactant(R)-2-Methyl-CBS-oxazaborolidineHCID 9838490—
ReactantHCID 86301334HCID 86301334—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
ProductHCID 86301484HCID 8630148456%

Reaction Conditions

Temperature-20 °C

Reaction Steps

To a cooled solution, −78° C., of 1-(7-((4-fluorobenzyl)oxy)quinolin-3-yl)ethanone (Example 42, 52 mg, 0.176 mmol) in toluene was added (R)-(+)-2-methyl-CBS-oxazaborolidine (97 mg, 0.352 mmol) followed by BH3.DMS (2 M in THF, 0.176 mL, 0.352 mmol). The reaction was warmed to −20° C. and stirred for 3 h followed by treatment with MeOH. The resulting mixture was warmed to ambient temperature and sat. NaHCO3 (aq.) solution was added. The aqueous layer was extracted with EtOAc and the combined organic fractions were washed with brine and concentrated under reduced pressure onto silica. Purification (FCC, SiO2, 0−5%, MeOH/DCM) afforded the title compound as a white solid (29 mg, 56%). 1H NMR (400 MHz, DMSO-d6) δ 8.85 (d, J=2.3 Hz, 1H), 8.20 (d, J=2.0 Hz, 1H), 7.93 (d, J=9.0 Hz, 1H), 7.61 (dd, J=5.5, 8.6 Hz, 2H), 7.51 (d, J=2.3 Hz, 1H), 7.33 (dd, J=2.5, 8.8 Hz, 1H), 7.28 (t, J=9.0 Hz, 2H), 5.44 (d, J=4.3 Hz, 1H), 5.29 (s, 2H), 5.01-4.91 (m, 1H), 1.47 (d, J=6.7 Hz, 3H). [M+H]=298.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150572B2
Source datasetuspto-grants-2015_10
ORD IDord-facec02aeba04eb99063bde946177a2a
Source noteuspto-grants-2015_10