Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670422Generated: October 31, 2026

Methyl iodide → tert-butyl [(3S)-1,5-dimethyl-2-oxo-2,3,4,5-tetrahydro-1H-1,5-benzodiazepin-3-yl]carbamate

https://huagongshe.com/reaction/1670422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactanttert-butyl ((S)-1-methyl-4-oxo-2,3,4,5-tetrahydro-1H-1,5-benzodiazepin-3-yl)carbamateHCID 57617722—
SolventTetrahydrofuranHCID 8028—
Producttert-butyl [(3S)-1,5-dimethyl-2-oxo-2,3,4,5-tetrahydro-1H-1,5-benzodiazepin-3-yl]carbamateHCID 57617768115.2%

Reaction Steps

36 mg of sodium hydride in suspension at 60% in oil (0.90 mmol) are introduced at −10° C. into a 50 mL round-bottomed flask, with stirring and under an argon atmosphere, containing 10 mL of THF and 265 mg of 11 (0.91 mmol). The medium is stirred for 1 h, and then 148 mg (1.04 mmol) of methyl iodide are added. The medium is kept stirring at RT for 24 h. The mixture is concentrated, and 320 mg of crude product are obtained, which product is chromatographed on a silica cartridge (50 g, eluent heptane/AcOEt—in an AcOEt gradient: 10 to 50%). 235 mg of expected product 17 are recovered.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994161B2
Source datasetuspto-grants-2011_08
ORD IDord-1a20521274b34d4d8acd53f44a70952b
Source noteuspto-grants-2011_08