Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

ChemicalBook CAS DataBase List Methyl 3-amino-7-methoxybenzo[b]thiophene-2-carboxylate

Methyl 3-amino-7-methoxybenzo[b]thiophene-2-carboxylate synthesis

4synthesis methods
2365-48-2 Synthesis
Methyl thioglycolate

2365-48-2
339 suppliers
$14.00/25g

198203-94-0 Synthesis
Benzonitrile, 2-fluoro-3-methoxy- (9CI)

198203-94-0
81 suppliers
inquiry

Methyl 3-amino-7-methoxybenzo[b]thiophene-2-carboxylate

198204-08-9
11 suppliers
inquiry

-

Yield:198204-08-9 94%

Reaction Conditions:

with potassium carbonate in N,N-dimethyl-formamide at 20; for 1.5 h;Inert atmosphere;

Steps:

A.A.1.A.1.12.A.1.12.7 A.1.12.7. Methyl 3-amino-7-methoxybenzo[b]thiophene-2-carboxylate

To a mixture of 2-fluoro-3-methoxybenzonitrile (7.000 g, 45.90 mmol) and potassium carbonate (12.802 g, 91.70 mmol) in DMF (50 mL) is added dropwise methyl 2-mercaptoacetate (4.53 mL, 48.10 mmol). The RM is stirred at RT, under nitrogen, for 1.5h. Water is then added, and the resulting suspension is filtered. The separated solid is then washed with water and dried under high vacuum to give methyl 3-amino-7- methoxybenzo[b]thiophene-2-carboxylate as a beige solid (10.200 g, 94%). LC-MS B: tR = 0.90 min; [M+H]+ = 238.07.

References:

WO2018/210987,2018,A1 Location in patent:Page/Page column 87

142596-50-7 Synthesis
3-Methoxy-2-Nitro Benzonitrile

142596-50-7
68 suppliers
inquiry

2365-48-2 Synthesis
Methyl thioglycolate

2365-48-2
339 suppliers
$14.00/25g

Methyl 3-amino-7-methoxybenzo[b]thiophene-2-carboxylate

198204-08-9
11 suppliers
inquiry

198204-64-7 Synthesis
2-fluoro-3-MethoxybenzaMide

198204-64-7
9 suppliers
inquiry

Methyl 3-amino-7-methoxybenzo[b]thiophene-2-carboxylate

198204-08-9
11 suppliers
inquiry