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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096214Generated: November 2, 2026

Sodium hydride → (Rac)-4-(tert-butyl-dimethyl-silanyloxy)-2-[7-oxo-4-(3-trifluoromethyl-phenyl)-[1,4]diazepan-1-yl]-butyric acid methyl ester

https://huagongshe.com/reaction/1096214

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantMonobasic potassium phosphateHCID 516951—
Reactant1-(3-Trifluoromethyl-phenyl)-[1,4]diazepan-5-oneHCID 21754509—
Reactant(Rac)-4-(tert-butyl-dimethyl-silanyloxy)-2-iodo-butyric acid methyl esterHCID 87149689—
SolventDimethylformamideHCID 6228—
Product(Rac)-4-(tert-butyl-dimethyl-silanyloxy)-2-[7-oxo-4-(3-trifluoromethyl-phenyl)-[1,4]diazepan-1-yl]-butyric acid methyl esterHCID 66783316217.3%

Reaction Steps

A solution of 1.60 g (1.94 mmol) of 1-(3-trifluoromethyl-phenyl)-[1,4]diazepan-5-one in 15 ml of DMF was treated at 0° C. with 0.33 g (7.44 mmol) of NaH (55% dispersion in oil). After 20 min at this temperature, the suspension was warmed to RT and added to a cooled solution (0° C.) of 2.33 g (6.50 mmol) of (rac)-4-(tert-butyl-dimethyl-silanyloxy)-2-iodo-butyric acid methyl ester (intermediate 1) in 15 ml of DMF. The solution was stirred 6 h at 0° C. and neutralized with cold 10% aq. KH2PO4 solution and extracted with Et2O (3×). The organic phases were washed with 10% aq. KH2PO4 solution, dried over Na2SO4 evaporated and purified by flash silica gel column (CH2Cl2:Et2O 4:1 to 2:1) to yield 2.06 g (68%) of the title compound as light yellow oil. MS: 489.2 (MH+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138175B2
Source datasetuspto-grants-2012_03
ORD IDord-71910e5679614fa8921bc7053889490f
Source noteuspto-grants-2012_03