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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420292Generated: November 2, 2026

Triethylamine → HCID 66649728, compound

https://huagongshe.com/reaction/420292

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPotassium vinyltrifluoroborateHCID 23679353—
ReactantHCID 57386048HCID 57386048—
CatalystHCID 178419112HCID 178419112—
Solvent1-PropanolHCID 1031—
ProductHCID 66649728HCID 66649728—

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of (3aR,7S,7aS)-7-(4-amino-3-fluoro-5-iodo-benzyl)-3-(3-tert-butyl-benzyl)-5,5-dioxo-hexahydro-1-oxa-5lambda*6*-thia-3-aza-inden-2-one (0.65 g, 1.1 mmol), NEt3 (0.54 mL, 3.9 mmol) and potassium vinyltrifluoroborate (0.39 g, 2.7 mmol) in n-propanol (20 mL) was added after degassing with argon (1,1′-bis(diphenylphosphino)ferrocene)-dichloro-palladium (0.063 g, 0.078 mmol) and the reaction mixture was heated at 90° C. for 3.5 h. After dilution with saturated NaHCO3 solution the product was extracted with EtOAc. Combined organic extracts were washed with brine, dried over MgSO4, filtered and evaporated. The title compound was obtained after chromatographic purification (Combi Flash, 40 g, hexane-EtOAc 5:95 to 0:100) as a yellow solid: TLC (toluene-EtOAc 3:1) Rf=0.38; UPLC RtD=1.756 min; ESIMS [M+NH4]+=504; 1H NMR (400 MHz, CDCl3): δ 7.38 (d, 1H), 7.30 (m, 2H). 7.09 (d, 1H), 6.80 (s, 1H), 6.72 (dd, 1H), 6.66 (d, 1H), 5.64 (d, 1H), 5.39 (d, 1H), 4.53 (d, 1H), 4.33 (d, 1H), 3.7-3.9 (m, 4H), 3.05 (m, 3H), 2.82 (dd, 1H), 2.72 (m, 1H), 2.60 (m, 2H), 1.31 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093406B2
Source datasetuspto-grants-2012_01
ORD IDord-616f9616ee744f10bd2d59c623e187e5
Source noteuspto-grants-2012_01