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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1717200Generated: November 4, 2026

Hexamethyldisilazane → HCID 59468964, compound

https://huagongshe.com/reaction/1717200

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexamethyldisilazaneHCID 13838—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
ReactantHCID 59468917HCID 59468917—
SolventDimethylformamideHCID 6228—
ProductHCID 59468964HCID 5946896473%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of (5R)-1-{[(1,1-dimethylethyl)oxy]carbonyl}-5-[4-{[(2-fluorophenyl)methyl]oxy}-3-(methyloxy)phenyl]-2-methyl-L-proline (D60, 150 mg, 0.33 mmol), diisopropylethyl amine (0.115 ml, 0.66 mmol) and TBTU (116 mg, 0.36 mmol) in dry DMF (5 ml) was stirred for 15 min at room temperature. HMDS (0.106 ml, 0.5 mmol) was added and stirring was continued at room temperature for 2 h. The mixture was cooled to 0° C. and saturated aqueous NaHCO3 solution was added and the resulting suspension was stirred for 30 min. The mixture was extracted with ethyl acetate and washed three times with ice cold brine. The organic layer was dried (Na2SO4), filtered and evaporated. The residue was purified by chromatography on silica gel using cyclohexane and ethyl acetate (8:2 to 7:3) to afford the title compound (110 mg, 73%); Rt (HPLC): 5.68 min; MS: (ES/+) m/z: 481 [M+Na] C25H31FN2O5 requires 458.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803833B2
Source datasetuspto-grants-2010_09
ORD IDord-b5bed72ac4a041da9ea4b7c915c1ba6d
Source noteuspto-grants-2010_09