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1030825-20-7
- Product Name:Canagliflozin Impurity
- Molecular Formula:C18H14BrFS
- Purity:99%
- Molecular Weight:361.278
Product Details;
CasNo: 1030825-20-7
Molecular Formula: C18H14BrFS
Manufacturer supply high quality Canagliflozin Impurity 1030825-20-7 with ISO standards
- Molecular Formula:C18H14BrFS
- Molecular Weight:361.278
- Melting Point:103 °C
- Boiling Point:438.3±40.0 °C(Predicted)
- PSA:28.24000
- Density:1.388
- LogP:6.21590
2-(5-Bromo-2-methylbenzyl)-5-(4-fluorophenyl)thiophene(Cas 1030825-20-7) Usage
InChI:InChI=1S/C18H14BrFS/c1-12-2-5-15(19)10-14(12)11-17-8-9-18(21-17)13-3-6-16(20)7-4-13/h2-10H,11H2,1H3
1030825-20-7 Relevant articles
METHOD FOR PRODUCING 5-BROMO-2-ALKYLBENZOIC ACID
-
Paragraph 0068; 0075-0078, (2021/09/03)
PROBLEM TO BE SOLVED: To provide a metho...
Preparation method of 2-(4-fluorophenyl)-5-[(5-bromo-2-methylphenyl)methyl]thiophene
-
Paragraph 0033; 0039-0040; 0042; 0046-0048; 0052-0054; 0058, (2020/06/17)
The invention relates to the technical f...
Preparation method of intermediate
-
Paragraph 0025; 0029, (2020/06/29)
The invention discloses a preparation me...
Preparation method for canagliflozin intermediate
-
, (2020/03/09)
The invention relates to a preparation m...
1030825-20-7 Process route
-
-
2-(4-fluorophenyl)-5-((5-amino-2-methylphenyl)methyl)thiophene

-
-
1030825-20-7
3-[[5-(4-fluorophenyl)-2-thienyl]methyl]-4-methylphenyl bromide
Conditions | Yield |
---|---|
2-(4-fluorophenyl)-5-((5-amino-2-methylphenyl)methyl)thiophene;
With
nitrous acid isobutyl ester; copper(I) bromide;
In
acetone;
for 1h;
Cooling with ice;
With
hydrogen bromide;
In
water;
at 90 ℃;
for 1h;
Temperature;
|
84% |
2-(4-fluorophenyl)-5-((5-amino-2-methylphenyl)methyl)thiophene;
With
nitrous acid isobutyl ester; copper(I) bromide;
In
acetone;
at -5 ℃;
for 1h;
With
hydrogen bromide;
In
water;
at 80 ℃;
for 2h;
Temperature;
|
82% |
-
-
58861-48-6
2-(4-fluorophenyl)thiophene

-
-
79669-49-1
5-bromo-2-methylbenzoic acid

-
-
1030825-20-7
3-[[5-(4-fluorophenyl)-2-thienyl]methyl]-4-methylphenyl bromide
Conditions | Yield |
---|---|
5-bromo-2-methylbenzoic acid;
With
thionyl chloride;
In
dichloromethane; N,N-dimethyl-formamide;
at 50 ℃;
for 1h;
With
titanium tetrachloride;
In
dichloromethane; N,N-dimethyl-formamide;
at 0 - 5 ℃;
for 0.416667h;
2-(4-fluorophenyl)thiophene;
In
dichloromethane; N,N-dimethyl-formamide;
at 5 ℃;
for 17h;
|
85.9% |
Multi-step reaction with 2 steps
1.1: thionyl chloride / N,N-dimethyl-formamide; dichloromethane / 0 - 35 °C
1.2: 0 - 35 °C
2.1: aluminum (III) chloride / tetrahydrofuran / 0.5 h / 0 - 5 °C
2.2: Reflux
With
aluminum (III) chloride; thionyl chloride;
In
tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
|
1030825-20-7 Upstream products
-
(5-bromo-2-methylphenyl)[5-(p-fluorophenyl)thiophene-2-yl]methanone
-
1-Bromo-4-fluorobenzene
-
2-(4-fluorophenyl)thiophene
-
5-bromo-2-methylbenzoyl?chloride
1030825-20-7 Downstream products
-
methyl 1-C-(3-{[5-(4-fluorophenyl)-2-thienyl]methyl}-4-methyl-phenyl)-D-glucopyranoside
-
(2-(4-fluorophenyl)-5-[(5-iodo-2-methylphenyl)methyl]thiophene)
-
(1R,4R,5S,6R)-4,5,6-tris(benzyloxy)-3-(benzyloxymethyl)-1-(3-((5-(4-fluorophenyl)thiophen-2-yl)methyl)-4-methylphenyl)cyclohex-2-enol
-
2,4-di-O-tert-butyldiphenylsilyl-1-C-(3-((5-(4-fluorophenyl)thiophen-2-yl)methyl)-4-methylphenyl)-β-D-glucopyranoside
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