5H-Pyridazino(3,4-b)(1,4)benzoxazine, 7-chloro-2-(2-diethylaminoethoxy)-10-(3-dimethylaminopropyl)-

Base Information

• Chemical Name: 5H-Pyridazino(3,4-b)(1,4)benzoxazine, 7-chloro-2-(2-diethylaminoethoxy)-10-(3-dimethylaminopropyl)-
• CAS No.: 62637-31-4
• Molecular Formula: C₂₁H₃₀ClN₅O₂
• Molecular Weight: 419.954
• DSSTox Substance ID: DTXSID40211693
• Nikkaji Number: J78.839B
• Wikidata: Q83086666
• Mol file: 62637-31-4.mol

Synonyms:BRN 1093666;5H-Pyridazino(3,4-b)(1,4)benzoxazine, 7-chloro-2-(2-diethylaminoethoxy)-10-(3-dimethylaminopropyl)-;62637-31-4;C21H30ClN5O2;DTXSID40211693;C21-H30-Cl-N5-O2;LS-129652;8-Chloro-3-(2-diethylaminoethoxy)-5-(3-dimethylaminopropyl)-5H-pyridazino[3,4-b][1,4]benzoxazine

Chemical Property of 5H-Pyridazino(3,4-b)(1,4)benzoxazine, 7-chloro-2-(2-diethylaminoethoxy)-10-(3-dimethylaminopropyl)-

Chemical Property:

• Vapor Pressure: 3.05E-13mmHg at 25°C
• Boiling Point: 575.4°Cat760mmHg
• Flash Point: 301.8°C
• Density: 1.183g/cm³
• XLogP3: 3.5
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 7
• Rotatable Bond Count: 10
• Exact Mass: 419.2088029
• Heavy Atom Count: 29
• Complexity: 482

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCN(CC)CCOC1=NN=C2C(=C1)N(C3=C(O2)C=C(C=C3)Cl)CCCN(C)C

Technology Process of 5H-Pyridazino(3,4-b)(1,4)benzoxazine, 7-chloro-2-(2-diethylaminoethoxy)-10-(3-dimethylaminopropyl)-

There total 3 articles about 5H-Pyridazino(3,4-b)(1,4)benzoxazine, 7-chloro-2-(2-diethylaminoethoxy)-10-(3-dimethylaminopropyl)- 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:

6-chlorobenzo[d]oxazol-2(3H)-one (19932-84-4) → 8-chloro-3-(2-diethylamino-ethoxy)-5-(3-dimethylamino-propyl)-5H-benzo[b]pyridazino[4,3-e][1,4]oxazine (62637-31-4)

Guidance literature:

Multi-step reaction with 2 steps

1: (i) NaOEt, EtOH, (ii) aq.KOH, (iii) /BRN= 124500/

2: (i) Na, xylene, (ii) /BRN= 1088753/

DOI:10.1007/BF00779120

Reference yield:

3-(dimethylamino)propyl chloride hydrochloride (5407-04-5) → 8-chloro-3-(2-diethylamino-ethoxy)-5-(3-dimethylamino-propyl)-5H-benzo[b]pyridazino[4,3-e][1,4]oxazine (62637-31-4)

Guidance literature:

Multi-step reaction with 2 steps

1: (i) NaOEt, EtOH, (ii) aq.KOH, (iii) /BRN= 124500/

2: (i) Na, xylene, (ii) /BRN= 1088753/

DOI:10.1007/BF00779120

Reference yield:

[3-(3,8-dichloro-benzo[b]pyridazino[4,3-e][1,4]oxazin-5-yl)-propyl]-dimethyl-amine (62637-25-6) + 2-(Diethylamino)ethanol (100-37-8) → 8-chloro-3-(2-diethylamino-ethoxy)-5-(3-dimethylamino-propyl)-5H-benzo[b]pyridazino[4,3-e][1,4]oxazine (62637-31-4)

Guidance literature:

Multistep reaction; (i) Na, xylene, (ii) /BRN= 1088753/;

DOI:10.1007/BF00779120

upstream raw materials:

[3-(3,8-dichloro-benzo[b]pyridazino[4,3-e][1,4]oxazin-5-yl)-propyl]-dimethyl-amine

2-(Diethylamino)ethanol

6-chlorobenzo[d]oxazol-2(3H)-one

3-(dimethylamino)propyl chloride hydrochloride