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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 930369Generated: October 29, 2026

Dicyclohexylcarbodiimide → HCID 86732191, compound

https://huagongshe.com/reaction/930369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantBenzoyl isothiocyanateHCID 68284—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 86732190HCID 86732190—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 86732191HCID 8673219158.6%

Reaction Steps

(2S,4S)-4-amino-4-(5-bromo-2-fluoropyridin-3-yl)-1,1,1,5-tetrafluoropentan-2-ol (2.83 g, 8.11 mmol) in MeCN (70 mL) was added benzoyl isothiocyanate (1.20 ml, 8.92 mmol) and the mixture was stirred at room temperature for 1 h. N,N′-dicyclohexylcarbodiimide (1.840 g, 8.92 mmol) and diisopropylethylamine (2.82 ml, 16.21 mmol) were added. The mixture was stirred at 50° C. for 7 h. The reaction was worked up with water and EtOAc. The separated organic layer was washed with brine, dried over sodium sulfate, filtered and concentrated. The crude material was purified by column chromatography using a gradient of 0-25% EtOAc/hexane to give N-((4S,6S)-4-(5-bromo-2-fluoropyridin-3-yl)-4-(fluoromethyl)-6-(trifluoromethyl)-5,6-dihydro-4H-1,3-oxazin-2-yl)benzamide (2.27 g, 4.75 mmol, 58.6% yield). MS m/z=479.8 [M+H]+. Calculated for C18H13BrF5N3O2: 478.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296734B2
Source datasetuspto-grants-2016_03
ORD IDord-bbdd2d1e83284f80ac2517ebe6f5ef7c
Source noteuspto-grants-2016_03