(5R)-1-{[(5R,6S)-5,6-bis(4-chlorophenyl)-3-isopropyl-6-methyl-5,6-dihydroimidazo[2,1-b][1,3]thiazol-2-yl]carbonyl}-5-methyl-L-proline

Base Information

Chemical Name:(5R)-1-{[(5R,6S)-5,6-bis(4-chlorophenyl)-3-isopropyl-6-methyl-5,6-dihydroimidazo[2,1-b][1,3]thiazol-2-yl]carbonyl}-5-methyl-L-proline
CAS No.:1033709-62-4
Molecular Formula:C₂₈H₂₉Cl₂N₃O₃S
Molecular Weight:558.529
Hs Code.:

Synonyms:(5R)-1-{[(5R,6S)-5,6-bis(4-chlorophenyl)-3-isopropyl-6-methyl-5,6-dihydroimidazo[2,1-b][1,3]thiazol-2-yl]carbonyl}-5-methyl-L-proline

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Chemical Property of (5R)-1-{[(5R,6S)-5,6-bis(4-chlorophenyl)-3-isopropyl-6-methyl-5,6-dihydroimidazo[2,1-b][1,3]thiazol-2-yl]carbonyl}-5-methyl-L-proline

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Technology Process of (5R)-1-{[(5R,6S)-5,6-bis(4-chlorophenyl)-3-isopropyl-6-methyl-5,6-dihydroimidazo[2,1-b][1,3]thiazol-2-yl]carbonyl}-5-methyl-L-proline

There total 7 articles about (5R)-1-{[(5R,6S)-5,6-bis(4-chlorophenyl)-3-isopropyl-6-methyl-5,6-dihydroimidazo[2,1-b][1,3]thiazol-2-yl]carbonyl}-5-methyl-L-proline 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: 69.0%

: 1033709-61-3
tert-butyl (5R)-1-{[(5R,6S)-5,6-bis(4-chlorophenyl)-3-isopropyl-6-methyl-5,6-dihydroimidazo[2,1-b][1,3]thiazol-2-yl]carbonyl}-5-methyl-L-prolinate

: 1033709-62-4
(5R)-1-{[(5R,6S)-5,6-bis(4-chlorophenyl)-3-isopropyl-6-methyl-5,6-dihydroimidazo[2,1-b][1,3]thiazol-2-yl]carbonyl}-5-methyl-L-proline

Guidance literature:: With methoxybenzene; trifluoroacetic acid; In chloroform; at 20 - 40 ℃; for 2h;
DOI:10.1016/j.bmc.2013.04.056

Reference yield:

: 32159-21-0
Cbz-L-pGlu-OH

: 1033709-62-4
(5R)-1-{[(5R,6S)-5,6-bis(4-chlorophenyl)-3-isopropyl-6-methyl-5,6-dihydroimidazo[2,1-b][1,3]thiazol-2-yl]carbonyl}-5-methyl-L-proline

Guidance literature:: Multi-step reaction with 7 steps

1.1: perchloric acid / water / 16 h / 20 °C

2.1: lithium triethylborohydride / tetrahydrofuran / 0.5 h / -78 °C / Inert atmosphere

3.1: toluene-4-sulfonic acid / 48 h / 20 °C

4.1: copper(I) bromide dimethylsulfide complex / diethyl ether / 0.5 h / -78 °C / Inert atmosphere

4.2: 16 h / -78 - 20 °C / Inert atmosphere

5.1: palladium 10% on activated carbon; hydrogen / methanol / 16 h / 20 °C / 760.05 Torr

6.1: triethylamine / tetrahydrofuran / 1 h / 20 °C / Cooling with ice

7.1: trifluoroacetic acid; methoxybenzene / chloroform / 2 h / 20 - 40 °C

With perchloric acid; copper(I) bromide dimethylsulfide complex; palladium 10% on activated carbon; hydrogen; lithium triethylborohydride; toluene-4-sulfonic acid; methoxybenzene; triethylamine; trifluoroacetic acid; In tetrahydrofuran; methanol; diethyl ether; chloroform; water;
DOI:10.1016/j.bmc.2013.04.056

Reference yield:

: a(2S)-1-benzyl 2-tert-butyl 5-hydroxypyrrolidine-1,2-dicarboxylate

: 1033709-62-4
(5R)-1-{[(5R,6S)-5,6-bis(4-chlorophenyl)-3-isopropyl-6-methyl-5,6-dihydroimidazo[2,1-b][1,3]thiazol-2-yl]carbonyl}-5-methyl-L-proline

Guidance literature:: Multi-step reaction with 5 steps

1.1: toluene-4-sulfonic acid / 48 h / 20 °C

2.1: copper(I) bromide dimethylsulfide complex / diethyl ether / 0.5 h / -78 °C / Inert atmosphere

2.2: 16 h / -78 - 20 °C / Inert atmosphere

3.1: palladium 10% on activated carbon; hydrogen / methanol / 16 h / 20 °C / 760.05 Torr

4.1: triethylamine / tetrahydrofuran / 1 h / 20 °C / Cooling with ice

5.1: trifluoroacetic acid; methoxybenzene / chloroform / 2 h / 20 - 40 °C

With copper(I) bromide dimethylsulfide complex; palladium 10% on activated carbon; hydrogen; toluene-4-sulfonic acid; methoxybenzene; triethylamine; trifluoroacetic acid; In tetrahydrofuran; methanol; diethyl ether; chloroform;
DOI:10.1016/j.bmc.2013.04.056