Carbamic acid, (10,11-dihydro-5-(1-oxo-3-(1-piperidinyl)propyl)-5H-dibenz(b,f)azepin-3-yl)-, methyl ester, monohydrochloride

Base Information

Chemical Name:Carbamic acid, (10,11-dihydro-5-(1-oxo-3-(1-piperidinyl)propyl)-5H-dibenz(b,f)azepin-3-yl)-, methyl ester, monohydrochloride
CAS No.:78816-53-2
Molecular Formula:C₂₄H₂₉N₃O₃*ClH
Molecular Weight:443.974
Hs Code.:
DSSTox Substance ID:DTXSID10229321

Synonyms:78816-53-2;Carbamic acid, (10,11-dihydro-5-(1-oxo-3-(1-piperidinyl)propyl)-5H-dibenz(b,f)azepin-3-yl)-, methyl ester, monohydrochloride;methyl N-[11-(3-piperidin-1-ylpropanoyl)-5,6-dihydrobenzo[b][1]benzazepin-2-yl]carbamate;hydrochloride;DTXSID10229321;C24-H29-N3-O3.Cl-H;AKOS030505588;LS-49371;LS-60361;methyl (5-(3-(piperidin-1-yl)propanoyl)-10,11-dihydro-5H-dibenzo[b,f]azepin-3-yl)carbamate hydrochloride

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Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of Carbamic acid, (10,11-dihydro-5-(1-oxo-3-(1-piperidinyl)propyl)-5H-dibenz(b,f)azepin-3-yl)-, methyl ester, monohydrochloride

Chemical Property:

Vapor Pressure:9.53E-14mmHg at 25°C
Boiling Point:586.7°C at 760 mmHg
Flash Point:308.6°C
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:443.1975695
Heavy Atom Count:31
Complexity:592

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC(=O)NC1=CC2=C(CCC3=CC=CC=C3N2C(=O)CCN4CCCCC4)C=C1.Cl

Technology Process of Carbamic acid, (10,11-dihydro-5-(1-oxo-3-(1-piperidinyl)propyl)-5H-dibenz(b,f)azepin-3-yl)-, methyl ester, monohydrochloride

There total 5 articles about Carbamic acid, (10,11-dihydro-5-(1-oxo-3-(1-piperidinyl)propyl)-5H-dibenz(b,f)azepin-3-yl)-, methyl ester, monohydrochloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 78816-52-1
3-Carbmethoxyamino-5-β-piperidinopropionyl-iminodibenzyl

: 78816-53-2
3-Carbmethoxyamino-5-β-piperidinopropionyl-iminodibenzyl-hydrochlorid

Guidance literature:: With hydrogenchloride; In isopropyl alcohol;

Reference yield:

: 110-89-4
piperidine

: 78816-53-2
3-Carbmethoxyamino-5-β-piperidinopropionyl-iminodibenzyl-hydrochlorid

Guidance literature:: Multi-step reaction with 2 steps

1: toluene / 4 h / 70 - 110.8 °C

2: HCl in isopropanol / propan-2-ol

With hydrogenchloride; In isopropyl alcohol; toluene;

Reference yield:

: 10464-35-4
3-amino-10,11-dihydro-5H-dibenzazepine

: 78816-53-2
3-Carbmethoxyamino-5-β-piperidinopropionyl-iminodibenzyl-hydrochlorid

Guidance literature:: Multi-step reaction with 4 steps

1: Na₂CO₃ / acetone; H₂O / 1.5 h

2: toluene / 4 h / Heating

3: toluene / 4 h / 70 - 110.8 °C

4: HCl in isopropanol / propan-2-ol

With hydrogenchloride; sodium carbonate; In water; isopropyl alcohol; acetone; toluene;