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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | 1,3-Thiazole-2-carbaldehyde | HCID 2734903 | — |
| Reactant | HCID 59511160 | HCID 59511160 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68690633 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07807671B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-9cf6b3d10ae4427ebf940631010d0832 |
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| Source note | uspto-grants-2010_10 |
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