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158299-05-9

158299-05-9 Structure

158299-05-9 Structure
IdentificationBack Directory
[Name]

3-(2-Bromo-1-oxopropyl)-spiro[2H-1,3-benzoxazine-2,1'-cyclohexan]-4(3H)-one
[CAS]

158299-05-9
[Synonyms]

BPSBC
BR-Comp
-cyclohexan]-4-one
3-(2-Bromo-1-oxoprop
Meropenem Intermediate
3-(2-bromopropanoyl)-3,4-dihydrospiro[1,3-benzoxazine-2,1'
3-isobutyrylspiro[benzo[e][1,3]oxazine-2,1'-cyclohexan]-4(3H)-one
3-(2-bromo-1-oxopropyl)-4-spiro[1,3-benzoxazine-2,1'-cyclohexane]one
3-(2-broMopropionyl)spiro[2H-1,3-benzoxazine-2,1'-cyclohexane]-4(3H)-one
3-(2-BroMopropanoyl)spiro[benzo[e][1,3]oxazine-2,1'-cyclohexan]-4(3H)-one
3-(2-BROMO-1-OXOPROPYL)-SPIRO[2H-1,3-BENZOXAZINE-2,1'-CYCLOHEXAN]-4(3H)-ONE
Spiro[2H-1,3-benzoxazine-2,1'-cyclohexan]-4(3H)-one, 3-(2-bromo-1-oxopropyl)-
3-(2-Bromo-1-oxopropyl)-spiro[2H-1,3-benzoxazine-2,1'-cyclohexan]-4(3H)-ketone
3-(2-Bromo-1-oxopropyl)-spiro[2H-1,3-benzoxazine-2,1'-cyclohexan]-4(3H)-one (BPSBC)
3-(2-Bromo-1-oxopropyl)-spiro[2H-1,3-benzoxazine-2,1'-cyclohexan]-4(3H)-one USP/EP/BP
3-(2-BroMo-1-oxopropyl)-spiro[2H-1,3-benzoxazine-2,1'-cyclohexan]-4(3H)-one (M2)
broMine propionyl snails benzoxazin cyclohexane-3-(2-broMine-generation-1-oxo-propyl)-Lo [2H-1,3-benzoxazine -2,1'-cyclohexane]-4(3H)-ketone
[EINECS(EC#)]

1806241-263-5
[Molecular Formula]

C16H18BrNO3
[MDL Number]

MFCD08458252
[MOL File]

158299-05-9.mol
[Molecular Weight]

352.22
Chemical PropertiesBack Directory
[Melting point ]

74-76 °C
[Boiling point ]

485.0±45.0 °C(Predicted)
[density ]

1.48±0.1 g/cm3(Predicted)
[Fp ]

247.1°C
[storage temp. ]

Inert atmosphere,2-8°C
[pka]

-2.33±0.20(Predicted)
[InChI]

InChI=1S/C16H18BrNO3/c1-11(17)14(19)18-15(20)12-7-3-4-8-13(12)21-16(18)9-5-2-6-10-16/h3-4,7-8,11H,2,5-6,9-10H2,1H3
[InChIKey]

APCHXTHKSJHPPE-UHFFFAOYSA-N
[SMILES]

O1C2=CC=CC=C2C(=O)N(C(=O)C(Br)C)C21CCCCC2
[CAS DataBase Reference]

158299-05-9
Safety DataBack Directory
[Symbol(GHS) ]

Corrosion (GHS05)Exclamation Mark (GHS07)Health Hazard (GHS08)Environment (GHS09)
GHS05,GHS07,GHS08,GHS09
[Signal word ]

Warning
[Hazard statements ]

H290-H302-H319-H334-H410
[Precautionary statements ]

P261-P264b-P270-P280i-P285-P301+P312-P304+P341-P305+P351+P338-P330-P337+P313-P342+P311-P390-P406b-P501c
Hazard InformationBack Directory
[Chemical Properties]

25KG
[Uses]

3-(2-Bromo-1-oxopropyl)-spiro[2h-1,3-benzoxazine-2,1'-cyclohexan]-4(3H)-one is an intermediate of meropenem, and meropenem is a carbapenem antibiotic, which is suitable for the treatment of meningitis.
[Application]

A useful research chemical compound.
[Synthesis]

spiro[3H-1,3-benzoxazine-2,1'-cyclohexane]-4-one

40033-95-2

2-Bromopropionyl bromide

563-76-8

3-(2-Bromo-1-oxopropyl)-spiro[2H-1,3-benzoxazine-2,1'-cyclohexan]-4(3H)-one

158299-05-9

Comparative Example 1: 1.4,80 g of spiro[benzo[e][1,3]oxazine-2,1'-cyclohexyl]-4(3H)-one, 127 g of 2-bromopropionyl bromide, and 40 g of pyridine (molar ratio 1:1.6:1) were dissolved in chlorobenzene (mass ratio 1:4.4). The mixture was placed in a four-necked flask under nitrogen protection and reacted at 50 °C for 8 hours. After completion of the reaction, the mixture was washed three times with 200 g of water, three times with 200 g of 10% potassium hydroxide solution and three times with 200 g of water, in that order. The organic phases were combined and concentrated under reduced pressure to remove the solvent to obtain a colorless liquid. To this liquid was added 80 g of ethanol (mass ratio 1:1), cooled to -5 °C, stirred for 2 h, filtered and dried to give 109 g of 3-(2-bromo-1-oxopropyl)-spiro[2H-1,3-benzoxazine-2,1 '-cyclohexyl]-4(3H)-one. The molar yield was 84.5% and the purity was 97.9%.

[storage]

Store the container tightly closed in a dry, cool and well-ventilated place. Store apart from foodstuff containers or incompatible materials.
[References]

[1] Journal of Organic Chemistry, 1995, vol. 60, # 5, p. 1096 - 1097
[2] Journal of the Chemical Society - Perkin Transactions 1, 1996, # 23, p. 2851 - 2856
[3] Journal of Organic Chemistry, 1997, vol. 62, # 9, p. 2877 - 2884
[4] Patent: CN106432122, 2017, A. Location in patent: Paragraph 0070-0072
[5] Patent: US5442055, 1995, A
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