ChemicalBook--->CAS DataBase List--->634468-96-5

634468-96-5

634468-96-5 Structure

634468-96-5 Structure
IdentificationBack Directory
[Name]

tert-butyl 4-(pyriMidin-5-yl)piperazine-1-carboxylate
[CAS]

634468-96-5
[Synonyms]

Nicotinamide Impurity 203
tert-butyl 4-(pyriMidin-5-yl)piperazine-1-carboxylate
1-Piperazinecarboxylic acid, 4-(5-pyrimidinyl)-, 1,1-dimethylethyl ester
[Molecular Formula]

C13H20N4O2
[MDL Number]

MFCD11872512
[MOL File]

634468-96-5.mol
[Molecular Weight]

264.32
Chemical PropertiesBack Directory
[storage temp. ]

Sealed in dry,Room Temperature
[Appearance]

Light brown to brown Solid
Spectrum DetailBack Directory
[Spectrum Detail]

tert-butyl 4-(pyriMidin-5-yl)piperazine-1-carboxylate(634468-96-5)1HNMR
Hazard InformationBack Directory
[Synthesis]

5-Bromopyrimidine

4595-59-9

1-BOC-Piperazine

57260-71-6

tert-butyl 4-(pyriMidin-5-yl)piperazine-1-carboxylate

634468-96-5

(1) Preparation of tert-butyl 4-(pyrimidin-5-yl)piperazine-1-carboxylate: a 100 mL aubergine flask was charged with 5-bromopyrimidine (3.16 g, 20 mmol), N-BOC-piperazine (3.72 g, 20 mmol), 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl (BINAP, 2.49 g, 4 mmol), cesium carbonate ( 13.0 g, 40 mmol) and tris(dibenzylideneacetone)dipalladium (Pd2(dba)3, 1.83 g, 2 mmol). Toluene (80 mL) was then added as solvent. The reaction mixture was heated to 90 °C and stirred for 12 h under the protection of nitrogen atmosphere. Upon completion of the reaction, the mixture was filtrated and the filtrate was concentrated under reduced pressure to remove the solvent. The crude product was purified by silica gel column chromatography with the eluent ratio of dichloromethane:methanol=50:1, and tert-butyl 4-(pyrimidin-5-yl)piperazine-1-carboxylate (3.1 g, 58.7% yield) was finally obtained.

[References]

[1] Tetrahedron Letters, 2006, vol. 47, # 15, p. 2549 - 2552
[2] Patent: EP3091008, 2016, A1. Location in patent: Paragraph 0380; 0381
[3] Patent: US2005/176722, 2005, A1. Location in patent: Page/Page column 20
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