5-(1-benzenesulfonyl-5-chloro-1H-pyrrolo[2,3-b]pyridin-3-ylmethyl)-4-chlorothiazol-2-ylamine

Base Information

Chemical Name:5-(1-benzenesulfonyl-5-chloro-1H-pyrrolo[2,3-b]pyridin-3-ylmethyl)-4-chlorothiazol-2-ylamine
CAS No.:1029052-69-4
Molecular Formula:C₁₇H₁₂Cl₂N₄O₂S₂
Molecular Weight:439.346
Hs Code.:

Synonyms:5-(1-benzenesulfonyl-5-chloro-1H-pyrrolo[2,3-b]pyridin-3-ylmethyl)-4-chlorothiazol-2-ylamine

Suppliers and Price of 5-(1-benzenesulfonyl-5-chloro-1H-pyrrolo[2,3-b]pyridin-3-ylmethyl)-4-chlorothiazol-2-ylamine

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 5-(1-benzenesulfonyl-5-chloro-1H-pyrrolo[2,3-b]pyridin-3-ylmethyl)-4-chlorothiazol-2-ylamine

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 5-(1-benzenesulfonyl-5-chloro-1H-pyrrolo[2,3-b]pyridin-3-ylmethyl)-4-chlorothiazol-2-ylamine

There total 5 articles about 5-(1-benzenesulfonyl-5-chloro-1H-pyrrolo[2,3-b]pyridin-3-ylmethyl)-4-chlorothiazol-2-ylamine 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: 74.2%

: 1029052-68-3
[5-(1-benzenesulfonyl-5-chloro-1H-pyrrolo[2,3-b]pyridin-3-ylmethyl)-4-chlorothiazol-2-yl]carbamic acid tert-butyl ester

: 1029052-69-4
5-(1-benzenesulfonyl-5-chloro-1H-pyrrolo[2,3-b]pyridin-3-ylmethyl)-4-chlorothiazol-2-ylamine

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; dichloromethane; at 20 ℃; for 48h;

Reference yield:

: 1029052-67-2
5-[(1-benzenesulfonyl-5-chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)hydroxymethyl]-4-chlorothiazol-2-ylcarbamic acid tert-butyl ester

: 1029052-69-4
5-(1-benzenesulfonyl-5-chloro-1H-pyrrolo[2,3-b]pyridin-3-ylmethyl)-4-chlorothiazol-2-ylamine

Guidance literature:: Multi-step reaction with 2 steps

1: triethylsilane; trifluoroacetic acid / dichloromethane / 3 h / 20 °C

2: hydrogenchloride / dichloromethane; 1,4-dioxane / 48 h / 20 °C

With hydrogenchloride; triethylsilane; trifluoroacetic acid; In 1,4-dioxane; dichloromethane;

Reference yield:

: 900514-08-1
5-chloro-3-iodo-1H-pyrrolo[2,3-b]pyridine

: 1029052-69-4
5-(1-benzenesulfonyl-5-chloro-1H-pyrrolo[2,3-b]pyridin-3-ylmethyl)-4-chlorothiazol-2-ylamine

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 15 h / 0 - 20 °C

2.1: isopropylmagnesium chloride / tetrahydrofuran / 0.67 h / -45 - -25 °C / Inert atmosphere

2.2: 2 h / -65 - 20 °C / Inert atmosphere

3.1: triethylsilane; trifluoroacetic acid / dichloromethane / 3 h / 20 °C

4.1: hydrogenchloride / dichloromethane; 1,4-dioxane / 48 h / 20 °C

With hydrogenchloride; triethylsilane; isopropylmagnesium chloride; sodium hydride; trifluoroacetic acid; In tetrahydrofuran; 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide; mineral oil;