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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486125Generated: November 4, 2026

Oxane-4-carbonyl chloride → tert-butyl(3S,4S)-7-cyano-1-((3-cyclopropylquinolin-4-yl)methyl)-4-methyl-2-oxo-5-(tetrahydro-2H-pyran-4-carbonyl)-2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazepin-3-ylcarbamate

https://huagongshe.com/reaction/1486125

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxane-4-carbonyl chlorideHCID 2795505—
Reactanttert-butyl(3S,4S)-7-cyano-1-((3-cyclopropylquinolin-4-yl)methyl)-4-methyl-2-oxo-2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazepin-3-ylcarbamateHCID 131736782—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
Producttert-butyl(3S,4S)-7-cyano-1-((3-cyclopropylquinolin-4-yl)methyl)-4-methyl-2-oxo-5-(tetrahydro-2H-pyran-4-carbonyl)-2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazepin-3-ylcarbamateHCID 11829272461%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a rt solution of tert-butyl(3S,4S)-7-cyano-1-((3-cyclopropylquinolin-4-yl)methyl)-4-methyl-2-oxo-2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazepin-3-ylcarbamate (93 mg, 187 μmol) in pyridine (374 μl) was added tetrahydro-2H-pyran-4-carbonyl chloride (139 mg, 935 μmol) dropwise. The reaction was stirred at 80° C. for 2 h, then cooled to rt, diluted with EtOAc, washed with H2O, sat. aq. NaHCO3, and sat. aq. NaCl, dried over Na2SO4, filtered, and concentrated. The crude material was purified by flash chromatography to provide tert-butyl(3S,4S)-7-cyano-1-((3-cyclopropylquinolin-4-yl)methyl)-4-methyl-2-oxo-5-(tetrahydro-2H-pyran-4-carbonyl)-2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazepin-3-ylcarbamate (69 mg, 61%) as an off-white solid. MS m/z 610 (MH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422331B2
Source datasetuspto-grants-2016_08
ORD IDord-79e12926b75f42a1a904559dcd27caef
Source noteuspto-grants-2016_08