ChemicalBook--->CAS DataBase List--->136310-64-0

136310-64-0

136310-64-0 Structure

136310-64-0 Structure
IdentificationBack Directory
[Name]

Scopine-2,2-dithienyl glycolate
[CAS]

136310-64-0
[Synonyms]

N-DeMethyl TiotropiuM
Tiotropium EP Impurity B
SCOPINE-2,2-DITHIENYL GLYCOLATE
Tiotropium Bromide EP Impurity B
Scopolamine 2-(2-thienyl)glycolate
CO base bis (2-thiophenyl) glycolate
Scopine-2,2-dithienyl glycolate USP/EP/BP
2-Thiopheneacetic acid, -hydroxy--2-thienyl-, (1,2,4,5,7)
Scopine di(2-thienyl)glycolate scopine-2-dithienyl glycolate
Tiotropium Bromide Impurity 2(Tiotropium Bromide EP Impurity B)
2-thiopheneacetic acid, a-hydroxy-a-2th ( Di(2-thienyl) Glycolate )
(1R,2R,4S,5S,7s)-9-Methyl-3-oxa-9-azatricyclo[3.3.1.02,4]nonan-7-yl 2-hydroxy-2,2-dithiophen-2-ylacetate
α-Hydroxy-α-2-thienyl-2-thiopheneacetic Acid (1α,2β,4β,5α,7β)-9-Methyl-3-oxa-9-azatricyclo[3.3.1.02,4]non-7-yl Ester
2-Thiopheneacetic acid, α-hydroxy-α-2-thienyl-, (1α,2β,4β,5α,7β)-9-methyl-3-oxa-9-azatricyclo[3.3.1.02,4]non-7-yl ester
[EINECS(EC#)]

603-953-6
[Molecular Formula]

C18H19NO4S2
[MDL Number]

MFCD09038796
[MOL File]

136310-64-0.mol
[Molecular Weight]

377.483
Chemical PropertiesBack Directory
[Melting point ]

138-140°C
[Boiling point ]

542.3±50.0 °C(Predicted)
[density ]

1.48±0.1 g/cm3(Predicted)
[storage temp. ]

-20°C Freezer
[solubility ]

Chloroform (Slightly), Methanol (Slightly, Heated)
[form ]

Solid
[pka]

10.32±0.29(Predicted)
[color ]

White to Off-White
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Hazard InformationBack Directory
[Chemical Properties]

Off-White Solid
[Uses]

Precursor to Tiotropium Bromide.
[Synthesis]

Methyl 2,2-dithienylglycolate

26447-85-8

Scopine

498-45-3

Scopine-2,2-dithienyl glycolate

136310-64-0

Example 1: 7 mol% NHC (relative to compound (1)) in THF at room temperature. In an anhydrous flask containing about 7.85 g of activated 4A molecular sieves, methyl 2,2-dithienylglycolate (2) (R = Me, 3.97 g, 15.6 mmol) and rel-(1R,2R,4S,5S,7s)-9-methyl-3-oxa-9-azatricyclo[3.3.1.02,4]nonan-7-ol (1) (2.61 g. 16.8 mmol) was dissolved in THF (14 mL). Another flask was taken and 1-butyl-3-methylimidazolium tetrafluoroborate (210 μL, 1.12 mmol), KOtBu/THF solution (960 μL, 0.96 mmol), and THF (1.0 mL) were added, and stirred for 15 min at room temperature. Subsequently, this mixture was transferred to a flask containing rel-(1R,2R,4S,5S,7s)-9-methyl-3-oxa-9-azatricyclo[3.3.1.02,4]nonan-7-ol solution using a syringe. The syringe and flask were washed with THF (2 x 0.5 mL) and the reaction mixture was stirred at room temperature for 18 h. HPLC analysis showed 86% yield of the expected product.After 18 h, the mixture was filtered and the molecular sieves were washed with THF (2 x 20 mL). The filtrate was concentrated to dryness and the residue was dissolved in toluene (30 mL) and 1M HCl (30 mL). Solid precipitation was observed during phase separation; the suspension was filtered and the solids were washed with toluene (30 mL) and redissolved in the separated aqueous phase. The aqueous phase suspension was cooled to 0 °C and alkalized to the proper pH by adding solid K2CO3. The mixture was stirred at 0 °C for about 30 min, and the resulting solid was filtered, washed with cold water, and dried first on a filter, followed by vacuum drying at 45 °C for 18 h to give the white solid product (3) (4.30 g, 73%, HPLC purity = 99.89%).

[References]

[1] Patent: WO2013/46138, 2013, A1. Location in patent: Page/Page column 9; 10
[2] Patent: US2004/242622, 2004, A1. Location in patent: Page 29
[3] ChemMedChem, 2017, vol. 12, # 15, p. 1173 - 1182
[4] Patent: US2014/303373, 2014, A1. Location in patent: Paragraph 0034; 0035; 0036; 0037
Questions And AnswerBack Directory
[Description]

Scopine-2,2-dithienyl glycolate is an organic compound. It is off-white solid. The melting point is 138-140°C. The storage temperature is -20°C. Scopine-2,2-dithienyl glycolate is one of the reaction intermediates in the preparation of tiotropium bromide, which is a highly effective anticholinergic agent and widely used for treatment of asthma and/or chronic obstructive pulmonary disease (COPD) (chronic obstructive pulmonary disease).

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