Carbamic acid, (10,11-dihydro-5-(3-(4-morpholinyl)-1-oxopropyl)-5H-dibenz(b,f)azepin-3-yl)-, 1-methylethyl ester, monohydrochloride

Base Information

Chemical Name:Carbamic acid, (10,11-dihydro-5-(3-(4-morpholinyl)-1-oxopropyl)-5H-dibenz(b,f)azepin-3-yl)-, 1-methylethyl ester, monohydrochloride
CAS No.:78816-61-2
Molecular Formula:C₂₅H₃₁N₃O₄*ClH
Molecular Weight:474
Hs Code.:
DSSTox Substance ID:DTXSID90229324
ChEMBL ID:CHEMBL1325437

Synonyms:78816-61-2;Carbamic acid, (10,11-dihydro-5-(3-(4-morpholinyl)-1-oxopropyl)-5H-dibenz(b,f)azepin-3-yl)-, 1-methylethyl ester, monohydrochloride;SMR000283622;MLS000687784;MLS003909528;C25H31N3O4.ClH;CHEMBL1325437;DTXSID90229324;C25-H31-N3-O4.Cl-H;AKOS030505156;LS-49369;SR-01000477667;SR-01000477667-1;Isopropyl {5-[3-(4-morpholinyl)propanoyl]-10,11-dihydro-5H-dibenzo[b,f]azepin-3-yl}carbamate hydrochloride

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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-(3-(4-morpholinyl)-1-oxopropyl)-5H-dibenz(b,f)azepin-3-yl)-, 1-methylethyl ester, monohydrochloride

Chemical Property:

Vapor Pressure:8.4E-15mmHg at 25°C
Boiling Point:609.6°C at 760 mmHg
Flash Point:322.5°C
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:6
Exact Mass:473.2081342
Heavy Atom Count:33
Complexity:637

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)OC(=O)NC1=CC2=C(CCC3=CC=CC=C3N2C(=O)CCN4CCOCC4)C=C1.Cl

Technology Process of Carbamic acid, (10,11-dihydro-5-(3-(4-morpholinyl)-1-oxopropyl)-5H-dibenz(b,f)azepin-3-yl)-, 1-methylethyl ester, monohydrochloride

There total 4 articles about Carbamic acid, (10,11-dihydro-5-(3-(4-morpholinyl)-1-oxopropyl)-5H-dibenz(b,f)azepin-3-yl)-, 1-methylethyl 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:

: 83275-59-6
3-Carbisopropoxyamino-5-β-morpholinopropionyl-iminodibenzyl

: 78816-61-2
3-Carbisopropoxyamino-5-β-morpholinopropionyl-iminodibenzyl-hydrochlorid

Guidance literature:: With hydrogenchloride; In isopropyl alcohol;

Reference yield:

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

: 78816-61-2
3-Carbisopropoxyamino-5-β-morpholinopropionyl-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;

Reference yield:

: 78816-59-8
3-Carbisopropoxyamino-10,11-dihydro-5H-dibenzazepin

: 78816-61-2
3-Carbisopropoxyamino-5-β-morpholinopropionyl-iminodibenzyl-hydrochlorid

Guidance literature:: Multi-step reaction with 3 steps

1: toluene / 4 h / Heating

2: toluene / 4 h / 70 - 110.8 °C

3: HCl in isopropanol / propan-2-ol

With hydrogenchloride; In isopropyl alcohol; toluene;