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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1157338Generated: November 2, 2026

Sodium bis(trimethylsilyl)amide → HCID 68690633, compound

https://huagongshe.com/reaction/1157338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant1,3-Thiazole-2-carbaldehydeHCID 2734903—
ReactantHCID 59511160HCID 59511160—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68690633HCID 68690633—

Reaction Steps

In a 100 ml 3 necked round bottle flask, tert-butyl 4-(cyano(diethoxyphosphoryl)methyl)piperazine-1-carboxylate (5.0 g) was taken in dry THF (25 ml) under nitrogen. Sodium bis trimethylsilyl amide (3.0 g) was added drop wise at 0° C. and stirred for 30 min, then thiazole-2-carboxaldehyde (1.60 g) in 15 ml dry THF was added drop wise to the above reaction mixture at 0° C. Reaction mixture was stirred at room temperature for overnight. TLC was checked no starting material and the reaction mixture was quenched with saturated ammonium chloride (50 ml) and ethyl acetate was added. The organic layer was washed with brine, dried and concentrated to get crude product tert-butyl 4-(1-cyano-2-(thiazol-2-yl)vinyl)piperazine-1-carboxylate as yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807671B2
Source datasetuspto-grants-2010_10
ORD IDord-9cf6b3d10ae4427ebf940631010d0832
Source noteuspto-grants-2010_10