{4-[(thiophene-2-carbonyl)-amino]-benzenesulfonylamino}-acetic acid methyl ester

Base Information

Chemical Name:{4-[(thiophene-2-carbonyl)-amino]-benzenesulfonylamino}-acetic acid methyl ester
CAS No.:208775-78-4
Molecular Formula:C₁₄H₁₄N₂O₅S₂
Molecular Weight:354.408
Hs Code.:

Synonyms:{4-[(thiophene-2-carbonyl)-amino]-benzenesulfonylamino}-acetic acid methyl ester

Suppliers and Price of {4-[(thiophene-2-carbonyl)-amino]-benzenesulfonylamino}-acetic acid methyl ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Total 1 raw suppliers

Chemical Property of {4-[(thiophene-2-carbonyl)-amino]-benzenesulfonylamino}-acetic acid methyl ester

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of {4-[(thiophene-2-carbonyl)-amino]-benzenesulfonylamino}-acetic acid methyl ester

There total 3 articles about {4-[(thiophene-2-carbonyl)-amino]-benzenesulfonylamino}-acetic acid methyl ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 83.0%

: 67-56-1
methanol

: 188005-80-3
N-[[4-(2-Thienylcarbonylamino)phenyl]sulfonyl]glycine

: 208775-78-4
{4-[(thiophene-2-carbonyl)-amino]-benzenesulfonylamino}-acetic acid methyl ester

Guidance literature:: With thionyl chloride; for 4h; Ambient temperature;
DOI:10.1007/BF02251685

Reference yield:

: 6846-13-5
N-phenyl-2-thiophenecarboxamide

: 208775-78-4
{4-[(thiophene-2-carbonyl)-amino]-benzenesulfonylamino}-acetic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 80 percent / chlorosulfonic acid / 40 °C

2: 88 percent / Et₃N / tetrahydrofuran; H₂O / 2 h / 20 °C

3: 83 percent / thionyl chloride / 4 h / Ambient temperature

With chlorosulfonic acid; thionyl chloride; triethylamine; In tetrahydrofuran; water;
DOI:10.1007/BF02251685

Reference yield:

: 108197-21-3
4-[(thiophene-2-carbonyl)-amino]-benzenesulfonyl chloride

: 208775-78-4
{4-[(thiophene-2-carbonyl)-amino]-benzenesulfonylamino}-acetic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 88 percent / Et₃N / tetrahydrofuran; H₂O / 2 h / 20 °C

2: 83 percent / thionyl chloride / 4 h / Ambient temperature

With thionyl chloride; triethylamine; In tetrahydrofuran; water;
DOI:10.1007/BF02251685