ChemicalBook > Product Catalog >Organic Chemistry >Heterocyclic Compounds >7-Bromoquinazoline-2,4(1H,3H)-dione

7-Bromoquinazoline-2,4(1H,3H)-dione

7-Bromoquinazoline-2,4(1H,3H)-dione Suppliers list
Company Name: Shanghai Kangenbo Medical Technology Co., Ltd.  Gold
Tel: 400-1388-521 17510465506
Email: renhuirong@kangenbo.cn
Company Name: Carbott PharmTech Inc.  
Tel: 0535-6385396
Email: info@carbottpharm.com
Company Name: Shangchem Co., Ltd.  
Tel: +86-21-68182121
Email:
Company Name: Pure Chemistry Scientific Inc.  
Tel: 001-857-928-2050 or 1-888-588-9418
Email: sales@chemreagents.com
Company Name: Adamas Reagent, Ltd.  
Tel: 400-6009262 15618770481
Email: yhx@titansci.com

7-Bromoquinazoline-2,4(1H,3H)-dione manufacturers

7-Bromoquinazoline-2,4(1H,3H)-dione Basic information
Product Name:7-Bromoquinazoline-2,4(1H,3H)-dione
Synonyms:7-Bromo-2,4(1H,3H)-quinazolinedione;7-Bromoquinazoline-2,4(1H,3H);7-bromo-1H-quinazoline-2,4-dione;7-bromo-1,2,3,4-tetrahydroquinazoline-2,4-dione;2,4(1H,3H)-Quinazolinedione, 7-bromo-;7-Bromoquinazoline-2,4(1H,3H)-dione/7-Bromo-2,4(1H,3H)-quinazolinedione;7-Bromoquinazoline-2,4(1H,3H)-Dione, 10 mM in DMSO;7-Bromoquinazoline-2,4-dione
CAS:114703-12-7
MF:C8H5BrN2O2
MW:241.04
EINECS:
Product Categories:
Mol File:114703-12-7.mol
7-Bromoquinazoline-2,4(1H,3H)-dione Structure
7-Bromoquinazoline-2,4(1H,3H)-dione Chemical Properties
Melting point >300℃
density 1.752±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka10.21±0.20(Predicted)
AppearanceLight yellow to green yellow Solid
Safety Information
MSDS Information
7-Bromoquinazoline-2,4(1H,3H)-dione Usage And Synthesis
Synthesis
Methyl 2-amino-4-bromobenzoate

135484-83-2

Sodium cyanate

917-61-3

7-BROMOQUINAZOLINE-2,4(1H,3H)-DIONE

114703-12-7

General procedure for the synthesis of 7-bromoquinazoline-2,4(1H,3H)-dione from methyl 2-amino-4-bromobenzoate and sodium cyanate: firstly, 87.0 g (1.33 mol) of sodium cyanate was added to 1.2 liters of acetic acid solution containing 269.0 g (1.17 mol) of methyl 2-amino-4-bromobenzoate and stirred at room temperature. Subsequently, the reaction mixture was continued to be stirred for 22 hours. Upon completion of the reaction, the reaction mixture was diluted with 1.5 liters of water and the solid residue was isolated by diafiltration. Next, 0.42 liters of 32% sodium hydroxide solution was added to the resulting solid and the mixture was diluted with 3.5 liters of water and subsequently heated on a steam bath for 4 hours. The reaction mixture was cooled and the solid residue was again separated by diafiltration. After conventional post-processing, 205.2 g of 7-bromo-1H-benzo[d]-1,3-oxazine-2,4-dione was finally obtained as a solid, which showed (M + H)+ = 243 by HPLC/MS.

References[1] Patent: US2013/12489, 2013, A1. Location in patent: Paragraph 0173
7-Bromoquinazoline-2,4(1H,3H)-dione Preparation Products And Raw materials
Raw materialsAcetamide-->Methyl 2-amino-4-bromobenzoate-->Sodium cyanate-->2-Amino-4-bromobenzoic acid-->Urea
Tag:7-Bromoquinazoline-2,4(1H,3H)-dione(114703-12-7) Related Product Information
7-Bromoquinazoline-2,4(1H,3H)-dione 8-bromoquinazoline-2,4(1H,3H)-dione 7-chloroquinazoline-2,4(1H,3H)-dione 5-bromoquinazolin-4-ol 4(3H)-Quinazolinone, 2-methoxy- 2,4-Dihydroxy quinazoline