tert-butyl 4-(4-chlorophenyl)-2-methyl-5-(4-((S)-5-methyl-5,7-dihydrothieno[3,4-d]pyrimidin-4-yl)piperazin-1-yl)-5-oxopentan-2-ylcarbamate

Base Information

Chemical Name:tert-butyl 4-(4-chlorophenyl)-2-methyl-5-(4-((S)-5-methyl-5,7-dihydrothieno[3,4-d]pyrimidin-4-yl)piperazin-1-yl)-5-oxopentan-2-ylcarbamate
CAS No.:1001124-02-2
Molecular Formula:C₂₈H₃₈ClN₅O₃S
Molecular Weight:560.16
Hs Code.:

Synonyms:tert-butyl 4-(4-chlorophenyl)-2-methyl-5-(4-((S)-5-methyl-5,7-dihydrothieno[3,4-d]pyrimidin-4-yl)piperazin-1-yl)-5-oxopentan-2-ylcarbamate

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Chemical Property of tert-butyl 4-(4-chlorophenyl)-2-methyl-5-(4-((S)-5-methyl-5,7-dihydrothieno[3,4-d]pyrimidin-4-yl)piperazin-1-yl)-5-oxopentan-2-ylcarbamate

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Technology Process of tert-butyl 4-(4-chlorophenyl)-2-methyl-5-(4-((S)-5-methyl-5,7-dihydrothieno[3,4-d]pyrimidin-4-yl)piperazin-1-yl)-5-oxopentan-2-ylcarbamate

There total 9 articles about tert-butyl 4-(4-chlorophenyl)-2-methyl-5-(4-((S)-5-methyl-5,7-dihydrothieno[3,4-d]pyrimidin-4-yl)piperazin-1-yl)-5-oxopentan-2-ylcarbamate 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: 58.0%

: 1001124-00-0
4-(tert-butoxycarbonylamino)-2-(4-chlorophenyl)-4-methylpentanoic acid

: (S)-5-methyl-4-(piperazin-1-yl)-5,7-dihydrothieno[3,4-d]pyrimidine hydrochloride

: 1001124-02-2
tert-butyl 4-(4-chlorophenyl)-2-methyl-5-(4-((S)-5-methyl-5,7-dihydrothieno[3,4-d]pyrimidin-4-yl)piperazin-1-yl)-5-oxopentan-2-ylcarbamate

Guidance literature:: With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine; In dichloromethane; at 20 ℃; for 1h;

Reference yield:

: 1001123-68-7
5-methyl-5,7-dihydrothieno[3,4-d]pyrimidin-4-ol

: 1001124-02-2
tert-butyl 4-(4-chlorophenyl)-2-methyl-5-(4-((S)-5-methyl-5,7-dihydrothieno[3,4-d]pyrimidin-4-yl)piperazin-1-yl)-5-oxopentan-2-ylcarbamate

Guidance literature:: Multi-step reaction with 5 steps

1.1: trichlorophosphate / 0.25 h / Heating / reflux

1.2: 1 h / 0 °C

2.1: 1-methyl-pyrrolidin-2-one / 120 °C

3.1: Resolution of racemate

4.1: hydrogenchloride / 1,4-dioxane; dichloromethane

5.1: O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine / dichloromethane / 1 h / 20 °C

With hydrogenchloride; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine; trichlorophosphate; In 1,4-dioxane; 1-methyl-pyrrolidin-2-one; dichloromethane;

Reference yield:

: 1001123-98-3
tert-butyl 4-(4-chlorophenyl)-2,2-dimethyl-5-oxopyrrolidine-1-carboxylate

: 1001124-02-2
tert-butyl 4-(4-chlorophenyl)-2-methyl-5-(4-((S)-5-methyl-5,7-dihydrothieno[3,4-d]pyrimidin-4-yl)piperazin-1-yl)-5-oxopentan-2-ylcarbamate

Guidance literature:: Multi-step reaction with 2 steps

1: methanol; lithium hydroxide; water / tetrahydrofuran / 20 °C

2: O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine / dichloromethane / 1 h / 20 °C

With methanol; lithium hydroxide; water; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine; In tetrahydrofuran; dichloromethane;