Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  API >  Antiallergic drugs >  Allergic Reactions >  Tiaramide

Tiaramide

Basic information Safety Supplier Related

Tiaramide Basic information

Product Name:
Tiaramide
Synonyms:
  • 1-Piperazineethanol, 4-((5-chloro-2-oxo-3(2H)-benzothiazolyl)acetyl)- (9ci)
  • 1-Piperazineethanol, 4-((5-chloro-2-oxo-3-benzothiazolinyl)acetyl)-
  • 35941-71-0 (Mono-hydrochloride)
  • 4-((5-Chloro-2-oxo-3(2H)-benzothiazolyl)acetyl)-1-piperazineethanol
  • 5-Chlor-2,3-dihydro-3-(4-(2-hydroxyethyl)piperazinylcarbonylmethyl)-2-benzothiazolon
  • Brn 1030245
  • Einecs 251-083-7
  • Rhc 2592a
CAS:
32527-55-2
MF:
C15H18ClN3O3S
MW:
355.84
EINECS:
251-083-7
Mol File:
32527-55-2.mol
More
Less

Tiaramide Chemical Properties

Melting point:
159-161 °C
Boiling point:
605.8±65.0 °C(Predicted)
Density 
1.432±0.06 g/cm3(Predicted)
pka
6.2(at 25℃)
More
Less

Tiaramide Usage And Synthesis

Originator

Solantal,Fujisawa,Japan,1975

Definition

ChEBI: Tiaramide is a member of benzothiazoles.

Manufacturing Process

A solution of ethyl 5-chloro-2-oxo-3-benzo-thiazolineacetate (4.0 grams) in 1- (2-hydroxyethyl)piperazine is heated at 100°C for 24 hours. After cooling, the resulting mixture is extracted with chloroform. The chloroform extract is washed with water and shaken with 10% hydrochloric acid. The hydrochloric acid layer is washed with chloroform, made alkaline with 10% sodium hydroxide solution and extracted with chloroform. The chloroform extract is washed with water, dried over magnesium sulfate and concentrated. The residual oil (5.5 grams) is allowed to stand to form crystals, which are recrystallized from a mixture of ethyl acetate (40 ml) and ethanol (15 ml) to give 3-[4-(2-hydroxyethyl)-1-piperazinylcarbonylmethyl]-5-chloro-2(3H)- benzothiazolinone (3.2 grams) as colorless crystals, MP 159° to 161°C. The following is an alternate method of preparation: A mixture of 3-(1- piperazinyl)carbonylmethyl-5-chloro-2(3H)-benzothiazolinone (500 mg), anhydrous potassium carbonate (400 mg), 2-hydroxyethyl bromide (300 mg) and anhydrous ethanol (20 ml) is heated while refluxing for 5 hours. The reaction mixture is concentrated under reduced pressure. The residue is extracted with chloroform. The chloroform layer is dried over magnesium sulfate and concentrated. The residue is crystallized from a mixture of ethyl acetate and ethanol to give 3-[4-(2-hydroxyethyl]-1- piperazinylcarbonylmethyl]-5-chloro-2(3H)-benzothiazolinone (370 mg) as crystals, MP 159° to 160°C.

Therapeutic Function

Antiinflammatory

TiaramideSupplier

Chengdu Kamel Pharmaceutical Co., Ltd
Tel
028-67136579 15828051124
Email
sales@kamelpharm.com
Dideu Industries Group Limited
Tel
+86-29-89586680 +86-15129568250
Email
1026@dideu.com
CONIER CHEM AND PHARMA LIMITED
Tel
+8618523575427
Email
sales@conier.com
Shaanxi Dideu Medichem Co. Ltd
Tel
+86-29-87569265 +86-18612256290
Email
1056@dideu.com
Bide Pharmatech Ltd.
Tel
400-1647117 15221909166
Email
product02@bidepharm.com