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Home > Encyclopedia > BMS 833923

BMS 833923

BMS 833923 structure

BMS 833923 

structure
  • CAS No:

    1059734-66-5

  • Formula:

    C30H27N5O

  • Chemical Name:

    BMS 833923

  • Synonyms:

    BMS 833923;XL 139;XL139;XL-139;BMS-833923 (XL-139);N-[2-Methyl-5-[(methylamino)methyl]phenyl]-4-[(4-phenylquinazolin-2-yl)amino]benzamide;Benzamide, N-[2-methyl-5-[(methylamino)methyl]phenyl]-4-[(4-phenyl-2-quinazolinyl)amino]-;BMS 833923 N-[2-Methyl-5-[(methylamino)methyl]phenyl]-4-[(4-phenylquinazolin-2-yl)amino]benzamide

  • Categories:

    Biochemical Engineering  >  Inhibitors

BMS 833923 Basic Attributes

473.56828

473.222

41J7ZJ239R

Characteristics

78.9

5.7

1.252±0.06 g/cm3(Predicted)

Drug Information

BMS-833923

BMS 833923 Use and Manufacturing

To a stirred suspension of 4-(4-phenylquinazolin-2-ylamino)benzoic acid (1.19 g, 3.49 mmol), prepared as described in Example 10, in dichloromethane (50 mL) was added a catalytic amount of dimethylformamide (100 μL) and thionyl chloride (1.50 mL, 20.6 mmol), and the resulting mixture was stirred at rt overnight. The solid was filtered, washed with hexanes, and dried under reduced pressure (high vacuum) to give the product (4-(4- phenylquinazolin-2-ylamino)benzoyl chloride) as a yellow solid (1.21 g, 97percent). This material was then added portionwise to a solution of commercially available 3-amino-4-methylbenzyl alcohol (600 mg, 4.37 mmol), and triethylamine (1.0 mL, 7.2 mmol) in dichloromethane (50 mL) that had been cooled to 0 To a stirred suspension of 4-(4-phenylquinazolin-2-ylamino)benzoic acid (1.19 g, 3.49 mmol), prepared as described in Example 10, in dichloromethane (50 mL) was added a catalytic amount of dimethylformamide (100 muL) and thionyl chloride (1.50 mL, 20.6 mmol), and the resulting mixture was stirred at rt overnight. The solid was filtered, washed with hexanes, and dried under reduced pressure (high vacuum) to give the product (4-(4- phenylquinazolin-2-ylamino)benzoyl chloride) as a yellow solid (1.21 g, 97%). This material was then added portionwise to a solution of commercially available 3-amino-4-methylbenzyl alcohol (600 mg, 4.37 mmol), and triethylamine (1.0 mL, 7.2 mmol) in dichloromethane (50 mL) that had been cooled to 0 0C in an ice bath. The mixture was allowed to warm to rt overnight, then the solid was collected by filtration, washed with saturated sodium bicarbonate and water and dried under reduced pressure to give 7V-(5- hydroxymethyl-2- methylphenyl)-4-(4-phenylquinazolin-2-ylamino)benzamide as a pure yellow solid (1.33 g, 86% o)).

Computed Properties

Molecular Weight:473.6
XLogP3:5.7
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:7
Exact Mass:473.22156050
Monoisotopic Mass:473.22156050
Topological Polar Surface Area:78.9
Heavy Atom Count:36
Complexity:689
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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