ChemicalBook--->CAS DataBase List--->140447-78-5

140447-78-5

140447-78-5 Structure

140447-78-5 Structure
IdentificationMore
[Name]

1-(2-N-Boc-Aminoethyl)piperazine
[CAS]

140447-78-5
[Synonyms]

1-(2-BOC-AMINOETHYL)PIPERAZINE
1-(2-N-BOC-AMINOETHYL)PIPERAZINE
(2-PIPERAZIN-1-YL-ETHYL)-CARBAMIC ACID TERT-BUTYL ESTER
ASINEX-REAG BAS 07746391
BUTTPARK 90\06-02
TIMTEC-BB SBB011604
1-(2-N-BOC-AMINOETHYL)PIPERAZINE 97%
[Molecular Formula]

C11H23N3O2
[MDL Number]

MFCD02683050
[Molecular Weight]

229.32
[MOL File]

140447-78-5.mol
Chemical PropertiesBack Directory
[Boiling point ]

357.2±27.0 °C(Predicted)
[density ]

1.014±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Sealed in dry,Store in freezer, under -20°C
[form ]

solid
[pka]

12.74±0.46(Predicted)
[color ]

White to off-white
[InChI]

InChI=1S/C11H23N3O2/c1-11(2,3)16-10(15)13-6-9-14-7-4-12-5-8-14/h12H,4-9H2,1-3H3,(H,13,15)
[InChIKey]

VPOIPCJBJNWHSJ-UHFFFAOYSA-N
[SMILES]

C(OC(C)(C)C)(=O)NCCN1CCNCC1
[CAS DataBase Reference]

140447-78-5(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H335-H315-H319
[Precautionary statements ]

P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
[WGK Germany ]

WGK 3
[HazardClass ]

IRRITANT
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Uses]

1-[2-(Boc-amino)ethyl]piperazine is used in preparation of dihydropyrimidine derivatives as bifunctional degraders for treatment and prophylaxis of target protein-mediated diseases.
[Synthesis]

1-CBZ-4-(2-N-BOC-AMINO-ETHYL)-PIPERAZINE

500013-42-3

1-(2-N-Boc-Aminoethyl)piperazine

140447-78-5

The general procedure for the synthesis of 1-(N-Boc-aminoethyl)piperazine from 1-CBZ-4-(BOC-aminoethyl)piperazine was as follows: hydrogen was vented into a degassed solution of benzyl 4-(2-(tert-butoxycarbonylamino)ethyl)piperazine-1-carboxylate (2.60 g, 7.16 mmol) containing 10% palladium carbon (500 mg) in methanol (50 ml), the reaction lasted for 2 hours. After completion of the reaction, the mixture was filtered through Celite. The filtrate was concentrated under vacuum to give a yellow colloidal product which was identified as tert-butyl 2-(1-piperazinyl)ethylcarbamate (1.60 g, 97% yield).

[References]

[1] Patent: EP1449844, 2004, A1. Location in patent: Page 34
[2] Organic and Biomolecular Chemistry, 2015, vol. 13, # 18, p. 5147 - 5157
Spectrum DetailBack Directory
[Spectrum Detail]

1-(2-N-Boc-Aminoethyl)piperazine(140447-78-5)1HNMR
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