2-(5-methyl-6-(2-(pyrrolidin-1-yIsulfonyl)benzyl)-4H-pyrrolo[2,3-d]thiazol-4-yl)acetic acid

Base Information

Chemical Name:2-(5-methyl-6-(2-(pyrrolidin-1-yIsulfonyl)benzyl)-4H-pyrrolo[2,3-d]thiazol-4-yl)acetic acid
CAS No.:1355613-49-8
Molecular Formula:C₁₉H₂₁N₃O₄S₂
Molecular Weight:419.525
Hs Code.:

Synonyms:2-(5-methyl-6-(2-(pyrrolidin-1-yIsulfonyl)benzyl)-4H-pyrrolo[2,3-d]thiazol-4-yl)acetic acid

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Chemical Property of 2-(5-methyl-6-(2-(pyrrolidin-1-yIsulfonyl)benzyl)-4H-pyrrolo[2,3-d]thiazol-4-yl)acetic acid

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Technology Process of 2-(5-methyl-6-(2-(pyrrolidin-1-yIsulfonyl)benzyl)-4H-pyrrolo[2,3-d]thiazol-4-yl)acetic acid

There total 5 articles about 2-(5-methyl-6-(2-(pyrrolidin-1-yIsulfonyl)benzyl)-4H-pyrrolo[2,3-d]thiazol-4-yl)acetic acid 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: 97.0%

: 1355613-61-4
ethyl 2-(5-methyl-6-(2-(pyrrolidin-1-ylsulfonyl)benzyl)-4H-pyrrolo[2,3-d]thiazol-4-yl)acetate

: 1355613-49-8
2-(5-methyl-6-(2-(pyrrolidin-1-yIsulfonyl)benzyl)-4H-pyrrolo[2,3-d]thiazol-4-yl)acetic acid

Guidance literature:: ethyl 2-(5-methyl-6-(2-(pyrrolidin-1-ylsulfonyl)benzyl)-4H-pyrrolo[2,3-d]thiazol-4-yl)acetate; With water; lithium hydroxide; In tetrahydrofuran; methanol; at 20 ℃; for 1h; Inert atmosphere;

With hydrogenchloride; In tetrahydrofuran; methanol; dichloromethane; water;

Reference yield:

: 1327366-69-7
5-methyl-4H-pyrrolo[2,3-d]thiazole

: 1355613-49-8
2-(5-methyl-6-(2-(pyrrolidin-1-yIsulfonyl)benzyl)-4H-pyrrolo[2,3-d]thiazol-4-yl)acetic acid

Guidance literature:: Multi-step reaction with 4 steps

1: sodium hydroxide; water / N,N-dimethyl-formamide / 25 - 55 °C

2: trimethylsilyl trifluoromethanesulfonate; triethylsilane / dichloromethane / 65 h / 0 °C

3: potassium carbonate; potassium iodide / acetonitrile / 3 h / 90 °C / Sealed vial; Inert atmosphere

4: water; lithium hydroxide / tetrahydrofuran; methanol / 1 h / 20 °C / Inert atmosphere

With triethylsilane; trimethylsilyl trifluoromethanesulfonate; water; potassium carbonate; potassium iodide; sodium hydroxide; lithium hydroxide; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 1355613-58-9
(5-methyl-4H-pyrroIo[2,3-d]thiazol-6-yl)(2-(pyrrolidin-1-ylsulfonyl)phenyI)methanol

: 1355613-49-8
2-(5-methyl-6-(2-(pyrrolidin-1-yIsulfonyl)benzyl)-4H-pyrrolo[2,3-d]thiazol-4-yl)acetic acid

Guidance literature:: Multi-step reaction with 3 steps

1: trimethylsilyl trifluoromethanesulfonate; triethylsilane / dichloromethane / 65 h / 0 °C

2: potassium carbonate; potassium iodide / acetonitrile / 3 h / 90 °C / Sealed vial; Inert atmosphere

3: water; lithium hydroxide / tetrahydrofuran; methanol / 1 h / 20 °C / Inert atmosphere

With triethylsilane; trimethylsilyl trifluoromethanesulfonate; water; potassium carbonate; potassium iodide; lithium hydroxide; In tetrahydrofuran; methanol; dichloromethane; acetonitrile;