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ChemicalBook--->CAS DataBase List--->112275-50-0

112275-50-0

112275-50-0 Structure

112275-50-0 Structure
IdentificationMore
[Name]

1-Boc-hexahydro-1,4-diazepine
[CAS]

112275-50-0
[Synonyms]

[1,4]DIAZEPANE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
1-BOC-1,4-DIAZEPANE
1-BOC-HEXAHYDRO-1,4-DIAZEPINE
1-BOC-HOMOPIPERAZINE
1-(TERT-BUTOXYCARBONYL)HOMOPIPERAZINE
BOC-HOMOPIPERAZINE
BOC-HOPAZ
BOC-HOPIZ
BUTTPARK 27\08-71
HPBOC
N-(T-BUTYLOXYCARBONYL)-HOMOPIPERAZINE
N-(TERT-BUTOXYCARBONYL)HOMOPIPERAZINE
N-(TERT-BUTYLOXYCARBONYL)-HOMOPIPERAZINE
TERT-BUTYL 1,4-DIAZEPANE-1-CARBOXYLATE
TERT-BUTYL 1-HOMOPIPERAZINECARBOXYLATE
TERT-BUTYL HOMOPIPERAZINE-1-CARBOXYLATE
1-(tert-Butoxycarbonyl)homopiperazine~tert-Butyl hexahydro-1,4-diazepine-1-carboxylate
Tert-butylhexahydro-1,4-diazepine-1-carboxylate
N-TERT-BUTYL-1-HOMOPIPERAZINE CARBOXYLATE
1-BOC-HOMOPIPERAZINE 98%
[EINECS(EC#)]

628-955-4
[Molecular Formula]

C10H20N2O2
[MDL Number]

MFCD00276987
[Molecular Weight]

200.28
[MOL File]

112275-50-0.mol
Chemical PropertiesBack Directory
[Melting point ]

143.4 °C
[Boiling point ]

95-110 °C0.5 mm Hg(lit.)
[density ]

1.016 g/mL at 20 °C(lit.)
[refractive index ]

n20/D 1.471(lit.)
[Fp ]

>230 °F
[storage temp. ]

Keep Cold
[form ]

Liquid
[pka]

10.45±0.20(Predicted)
[color ]

Colorless to yellow
[Specific Gravity]

1.016
[Water Solubility ]

Not miscible or difficult to mix in water.
[Sensitive ]

Air Sensitive
[Detection Methods]

GC,NMR,MS
[BRN ]

7581789
[CAS DataBase Reference]

112275-50-0(CAS DataBase Reference)
Safety DataBack Directory
[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:Wear suitable protective clothing .
[RIDADR ]

2735
[WGK Germany ]

3
[F ]

10-34
[Hazard Note ]

Irritant
[HazardClass ]

8
[HazardClass ]

IRRITANT, KEEP COLD
[HS Code ]

29339900
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Ethanol-->Sodium hydroxide-->Hydrochloric acid-->Ethyl acetate-->Methanol-->Diethyl ether-->Sulfuric acid-->Acetic acid-->Sodium-->Toluene-->Potassium carbonate-->Chloroform-->Sodium sulfate-->Magnesium sulfate-->Potassium hydroxide-->Acetone-->Sodium bicarbonate-->Hydrogen bromide-->Di-tert-butyl dicarbonate-->1-Butanol-->Sodium acetate-->Phenol-->Tosyl chloride-->Ethylenediamine-->Homopiperazine-->tert-Butyl methyl ether-->Sulfurous Acid-->Tetrabutylammonium fluoride-->1,3-Dibromopropane-->Benzhydrylamine-->Benzyltriethylammonium bromide-->N,N'-Bis(ethylene)-p-Toluenesulfonamide-->t-butyl chloroformate
Hazard InformationBack Directory
[Chemical Properties]

Colorless to yellow liquid
[Uses]

1-Boc-hexahydro-1,4-diazepine is a diazepine derivative used in the preparation of pharmaceutical compounds such as histamine H3-receptor antagonists and dipeptidyl peptidase IV (DPP-IV) inhibitors.
[Application]

1-Boc-homopiperazine is used in synthesis of potent anticoagulant. It is also used to produce 4-(7,8,9,10-tetrahydro-6H-cyclohepta[b]quinolin-11-yl)-[1,4]diazepane-1-carboxylic acid tert-butyl ester by reaction with 11-bromo-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinoline.
[General Description]

1-Boc-hexahydro-1,4-diazepine is an N-boc protected homopiperazine. Its enthalpy of vaporization at boiling point (558.15K) is 49.498kjoule/mol.
[Synthesis]

To a solution of di-tert-butyldicarbonate (2.201 g, 9.780 mmol) in acetic acid (9.8 mL), a solution of 1,4-diazepane (1.0 g, 9.780 mmol) in acetic acid (9.8 mL) is added at room temperature. After 24 hours, water is added and the pH is adjusted to 10 using 10% NaOH. The aqueous phase is then extracted with dichloromethane (2 x 15 mL). The organic phase is dried and the solvent is evaporated to obtain tert-butyl 1,4-diazepane-1-carboxylate (1-Boc-hexahydro-1,4-diazepine) with a yield of 90.0%.1-Boc-hexahydro-1,4-diazepine
[Precautions]

Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store under inert gas. It is sensitive to air.
[References]

Synthesis and biological activity of novel 1,4-diazepane derivatives as factor Xa inhibitor with potent anticoagulant and antithrombotic activity. Bioorganic &Medicinal Chemistry. 2004, 12 (9), 2179-2191.
Discovery and structure-activity relationship of thienopyridine derivatives as bone anabolic agents. Bioorganic & medicinal chemistry. 2013, 21 (7), 1628-1642.
Spectrum DetailBack Directory
[Spectrum Detail]

1-Boc-hexahydro-1,4-diazepine(112275-50-0)1HNMR
1-Boc-hexahydro-1,4-diazepine(112275-50-0)IR
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

tert-butyl 1,4-diazepane-1-carboxylate(112275-50-0)
[Alfa Aesar]

1-Boc-homopiperazine, 98%(112275-50-0)
[Sigma Aldrich]

112275-50-0(sigmaaldrich)
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