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Home > Encyclopedia > 2,5-DIBROMOTHIAZOLE

2,5-DIBROMOTHIAZOLE

2,5-DIBROMOTHIAZOLE structure

2,5-DIBROMOTHIAZOLE 

structure
  • CAS No:

    4175-78-4

  • Formula:

    C3HBr2NS

  • Chemical Name:

    2,5-DIBROMOTHIAZOLE

  • Synonyms:

    NSC222407;2,5-DIBROMOTHIAZOLE;Thiazole,2,5-dibroMo-;2,5-Dibromothiazole,97%;2,5-DIBROMOTHIAZOLE95%;2,5-Dibromo-1,3-thiazole

  • Categories:

    Pharmaceutical Intermediates  >  Bulk Drug Intermediates

Description

White to brown crystalline powder

2,5-DIBROMOTHIAZOLE Basic Attributes

242.916

240.819626

222407

DTXSID40310094

2934100090

Characteristics

41.1

3

2.3±0.1 g/cm3

45-49 °C(lit.)

242.8°C at 760 mmHg

100.6±19.8 °C

1.650

Safety Information

NONH for all modes of transport

3

R36/37/38

S26-S36

Xi: Irritant;

P261-P305 + P351 + P338

H315-H319-H335

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 46 companies from 5 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

2,5-DIBROMOTHIAZOLE Use and Manufacturing

Methods of Manufacturing

A solution of 2-amino-5-bromothiazole (1-21) (5.5 g, 30.72 mmol) in acetonitrile (50 mL) was treated with copper (II) bromide (3.43 g, 15.36 mmol) and isoamyl nitrite (4.9 mL, 36.87 mmol), and the resulting reaction mixture was heated at 60°C for 4 hours. The volatiles were removed by evaporation, and the obtained residue was diluted with water (50 mL) , followed by extraction with ethyl acetate (25 mL x 2), The combined organic layers were washed with brine (50 mL) , dried over anhydrous Na2S04 and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (60-120 mesh) using 10percent EtOAc in hexanes to give the desired product 1-22 (5.05 g, 68percent) as a yellow liquid; LCMS : m/z 243.6 [M+2].Step I: 2, 5-dibromothiazole (1-22) Compound thiazole (1 mmol, 84.9 mg)Carbon tetrabromide (2.1 mmol, 696.4 mg) was placed in a 10 mL round bottom flask.Added 5 mL of N, N-dimethylformamide and sodium tert-butoxide (4.0 mmol, 384.4 mg).Stir at room temperature for 3 hours, TLC monitored the endpoint of the reaction.The mixture was poured into water and extracted with dichloromethane. The organic phase was collected and dried. The dichloromethane was removed by rotary evaporation at low temperature to obtain a crude product.The crude product was subjected to silica gel column chromatography with petroleum ether and ethyl acetate as eluent (volume ratio = 30:1).2, 5-Dibromothiazole (colorless liquid, slow crystallisation at low temperature, 186.4 mg, yield 77percent) was obtained.

Uses

Used as a building block in material science.1,2 2,5-Dibromothiazole is used in the preparation of arylthiazolylpiperidine derivatives and analogs for use as survival motor neuron (SMN) protein production modulators.

Computed Properties

Molecular Weight:242.92
XLogP3:3
Hydrogen Bond Acceptor Count:2
Exact Mass:242.81760
Monoisotopic Mass:240.81965
Topological Polar Surface Area:41.1
Heavy Atom Count:7
Complexity:70
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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