tert-butyl N-[3-[1-(3-benzyl-4-oxothieno[3,2-d]pyrimidin-2-yl)propyl-(4-methylbenzoyl)amino]propyl]carbamate

Base Information

Chemical Name:tert-butyl N-[3-[1-(3-benzyl-4-oxothieno[3,2-d]pyrimidin-2-yl)propyl-(4-methylbenzoyl)amino]propyl]carbamate
CAS No.:1333403-61-4
Molecular Formula:C₃₂H₃₈N₄O₄S
Molecular Weight:574.744
Hs Code.:

Synonyms:tert-butyl N-[3-[1-(3-benzyl-4-oxothieno[3,2-d]pyrimidin-2-yl)propyl-(4-methylbenzoyl)amino]propyl]carbamate

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Chemical Property of tert-butyl N-[3-[1-(3-benzyl-4-oxothieno[3,2-d]pyrimidin-2-yl)propyl-(4-methylbenzoyl)amino]propyl]carbamate

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Technology Process of tert-butyl N-[3-[1-(3-benzyl-4-oxothieno[3,2-d]pyrimidin-2-yl)propyl-(4-methylbenzoyl)amino]propyl]carbamate

There total 7 articles about tert-butyl N-[3-[1-(3-benzyl-4-oxothieno[3,2-d]pyrimidin-2-yl)propyl-(4-methylbenzoyl)amino]propyl]carbamate 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: 93.0%

: 1333404-70-8
tert-butyl N-[3-[1-(3-benzyl-4-oxothieno[3,2-d]pyrimidin-2-yl)propylamino]propyl]carbamate

: 874-60-2
4-methyl-benzoyl chloride

: 1333403-61-4
tert-butyl N-[3-[1-(3-benzyl-4-oxothieno[3,2-d]pyrimidin-2-yl)propyl-(4-methylbenzoyl)amino]propyl]carbamate

Guidance literature:: With triethylamine; In dichloromethane; at 25 ℃; for 0.5h;
DOI:10.1021/jm200629m

Reference yield:

: 545379-50-8
3-benzyl-2-(1-bromopropyl)thieno[2,3-e]pyrimidin-4-one

: 1333403-61-4
tert-butyl N-[3-[1-(3-benzyl-4-oxothieno[3,2-d]pyrimidin-2-yl)propyl-(4-methylbenzoyl)amino]propyl]carbamate

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / N,N-dimethyl-formamide / 1 h / 55 °C

2: triethylamine / dichloromethane / 0.5 h / 25 °C

With potassium carbonate; triethylamine; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm200629m

Reference yield:

: 158806-49-6
methyl 3-(butanoylamino)thiophene-2-carboxylate

: 1333403-61-4
tert-butyl N-[3-[1-(3-benzyl-4-oxothieno[3,2-d]pyrimidin-2-yl)propyl-(4-methylbenzoyl)amino]propyl]carbamate

Guidance literature:: Multi-step reaction with 5 steps

1: ammonium hydroxide / 3 h / 105 °C

2: potassium carbonate / N,N-dimethyl-formamide / 12 h / 25 °C

3: bromine; sodium acetate; acetic acid / 55 °C

4: potassium carbonate / N,N-dimethyl-formamide / 1 h / 55 °C

5: triethylamine / dichloromethane / 0.5 h / 25 °C

With ammonium hydroxide; bromine; sodium acetate; potassium carbonate; acetic acid; triethylamine; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm200629m