1-{5-(2-chloropyridin-3-yl)-4-fluoro-1-[(3-fluorophenyl)sulfonyl]-1H-pyrrol-3-yl}-N-methylmethanamine hydrochloride

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Chemical Name:1-{5-(2-chloropyridin-3-yl)-4-fluoro-1-[(3-fluorophenyl)sulfonyl]-1H-pyrrol-3-yl}-N-methylmethanamine hydrochloride
CAS No.:1055305-25-3
Molecular Formula:C₁₇H₁₄ClF₂N₃O₂S*ClH
Molecular Weight:434.294
Hs Code.:

Synonyms:1-{5-(2-chloropyridin-3-yl)-4-fluoro-1-[(3-fluorophenyl)sulfonyl]-1H-pyrrol-3-yl}-N-methylmethanamine hydrochloride

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Chemical Property of 1-{5-(2-chloropyridin-3-yl)-4-fluoro-1-[(3-fluorophenyl)sulfonyl]-1H-pyrrol-3-yl}-N-methylmethanamine hydrochloride

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Technology Process of 1-{5-(2-chloropyridin-3-yl)-4-fluoro-1-[(3-fluorophenyl)sulfonyl]-1H-pyrrol-3-yl}-N-methylmethanamine hydrochloride

There total 11 articles about 1-{5-(2-chloropyridin-3-yl)-4-fluoro-1-[(3-fluorophenyl)sulfonyl]-1H-pyrrol-3-yl}-N-methylmethanamine hydrochloride 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: 63.0%

: 1055306-92-7
tert-butyl ({5-(2-chloropyridin-3-yl)-4-fluoro-1-[(3-fluorophenyl)sulfonyl]-1H-pyrrol-3-yl}methyl)methylcarbamate

: 1055305-25-3
1-{5-(2-chloropyridin-3-yl)-4-fluoro-1-[(3-fluorophenyl)sulfonyl]-1H-pyrrol-3-yl}-N-methylmethanamine hydrochloride

Guidance literature:: With hydrogenchloride; isopropyl alcohol; In ethyl acetate; at 20 ℃; for 3h;

Reference yield:

: 1055306-63-2
tert-butyl (4RS)-4-(bromomethyl)-3,3-difluoro-2-oxopyrrolidine-1-carboxylate

: 1055305-25-3
1-{5-(2-chloropyridin-3-yl)-4-fluoro-1-[(3-fluorophenyl)sulfonyl]-1H-pyrrol-3-yl}-N-methylmethanamine hydrochloride

Guidance literature:: Multi-step reaction with 9 steps

1.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / tetrahydrofuran / 1.25 h / 0 - 20 °C

2.1: n-butyllithium; diisopropylamine / tetrahydrofuran; hexane / 2.75 h / -78 °C

2.2: 3 h / -78 °C

3.1: hydrogenchloride; water; acetic acid / 1 h / 20 °C

4.1: sodium hydride / tetrahydrofuran / 16 h / 0 - 60 °C

4.2: 0.5 h / 0 °C

5.1: sodium hydride / tetrahydrofuran / 0.25 h / 0 °C

5.2: 0.5 h / 0 °C

6.1: carbonochloridic acid 1-chloro-ethyl ester / tetrahydrofuran / 1 h / 0 °C

6.2: 14 h / 0 °C / Heating / reflux

6.3: 1 h / 20 °C

7.1: methanol; sodium hydroxide; water; isopropyl alcohol / tetrahydrofuran / 1 h / 20 °C

8.1: 15-crown-5; sodium hydride / tetrahydrofuran / 0.17 h / 0 °C

9.1: hydrogenchloride; isopropyl alcohol / ethyl acetate / 3 h / 20 °C

With hydrogenchloride; methanol; sodium hydroxide; n-butyllithium; 15-crown-5; carbonochloridic acid 1-chloro-ethyl ester; water; sodium hydride; acetic acid; 1,8-diazabicyclo[5.4.0]undec-7-ene; diisopropylamine; isopropyl alcohol; In tetrahydrofuran; hexane; ethyl acetate;

Reference yield:

: 1055306-70-1
tert-butyl [4-(2-chloropyridin-3-yl)-3,3-difluoro-2-methylene-4-oxobutyl]carbamate

: 1055305-25-3
1-{5-(2-chloropyridin-3-yl)-4-fluoro-1-[(3-fluorophenyl)sulfonyl]-1H-pyrrol-3-yl}-N-methylmethanamine hydrochloride

Guidance literature:: Multi-step reaction with 7 steps

1.1: hydrogenchloride; water; acetic acid / 1 h / 20 °C

2.1: sodium hydride / tetrahydrofuran / 16 h / 0 - 60 °C

2.2: 0.5 h / 0 °C

3.1: sodium hydride / tetrahydrofuran / 0.25 h / 0 °C

3.2: 0.5 h / 0 °C

4.1: carbonochloridic acid 1-chloro-ethyl ester / tetrahydrofuran / 1 h / 0 °C

4.2: 14 h / 0 °C / Heating / reflux

4.3: 1 h / 20 °C

5.1: methanol; sodium hydroxide; water; isopropyl alcohol / tetrahydrofuran / 1 h / 20 °C

6.1: 15-crown-5; sodium hydride / tetrahydrofuran / 0.17 h / 0 °C

7.1: hydrogenchloride; isopropyl alcohol / ethyl acetate / 3 h / 20 °C

With hydrogenchloride; methanol; sodium hydroxide; 15-crown-5; carbonochloridic acid 1-chloro-ethyl ester; water; sodium hydride; acetic acid; isopropyl alcohol; In tetrahydrofuran; ethyl acetate;