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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372937Generated: October 31, 2026

Methyl iodide → HCID 69038045, compound

https://huagongshe.com/reaction/1372937

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactanttert-butyl N-[(3S)-2-oxo-2,3,4,5-tetrahydro-1H-1,5-benzodiazepin-3-yl]carbamateHCID 22881971—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69038045HCID 6903804594.4%

Reaction Conditions

Temperature-75 °C

Reaction Steps

To a solution of 5.0 g (18 mmol) (S)-(2-oxo-2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazepin-3-yl)-carbamic acid tert-butyl ester in 80 ml of tetrahydrofuran at −75° C. 18 ml (18 mmol) of lithium bis(trimethylsilyl)amide solution (1M in tetrahydrofurane) was added. After stirring for 30 min at −75° C. the mixture was allowed to reach room temperature and 3.07 g (21.6 mmol) of methyl iodide was added. The mixture was stirred for 2.5 hours at room temperature and concentrated in vacuo. The residue was distributed between 1M NaHSO4 solution and ethyl acetate. The combined organic layers were reextracted with water and dried (MgSO4) to yield 4.95 g (94%) of (1-methyl-2-oxo-2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazepin-3-yl)-carbamic acid tert-butyl ester as a white foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07160875B2
Source datasetuspto-grants-2007_01
ORD IDord-cac02c74ff5246cc96a3bfb7d9109a0d
Source noteuspto-grants-2007_01