(3-{[(RS)-1-(6-benzyl-3-chloro-2-methyl-7-oxo-6,7-dihydro-pyrazolo[1,5-c]pyrimidin-5-yl)-2-methyl-propyl]-[(4-trifluoromethyl-phenyl)-carbonyl]-amino}-propyl)-carbamic acid tert-butyl ester

Base Information

Chemical Name:(3-{[(RS)-1-(6-benzyl-3-chloro-2-methyl-7-oxo-6,7-dihydro-pyrazolo[1,5-c]pyrimidin-5-yl)-2-methyl-propyl]-[(4-trifluoromethyl-phenyl)-carbonyl]-amino}-propyl)-carbamic acid tert-butyl ester
CAS No.:960292-17-5
Molecular Formula:C₃₄H₃₉ClF₃N₅O₄
Molecular Weight:674.163
Hs Code.:

(3-{[(RS)-1-(6-benzyl-3-chloro-2-methyl-7-oxo-6,7-dihydro-pyrazolo[1,5-c]pyrimidin-5-yl)-2-methyl-propyl]-[(4-trifluoromethyl-phenyl)-carbonyl]-amino}-propyl)-carbamic acid tert-butyl ester

Synonyms:(3-{[(RS)-1-(6-benzyl-3-chloro-2-methyl-7-oxo-6,7-dihydro-pyrazolo[1,5-c]pyrimidin-5-yl)-2-methyl-propyl]-[(4-trifluoromethyl-phenyl)-carbonyl]-amino}-propyl)-carbamic acid tert-butyl ester

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Chemical Property of (3-{[(RS)-1-(6-benzyl-3-chloro-2-methyl-7-oxo-6,7-dihydro-pyrazolo[1,5-c]pyrimidin-5-yl)-2-methyl-propyl]-[(4-trifluoromethyl-phenyl)-carbonyl]-amino}-propyl)-carbamic acid tert-butyl ester

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Technology Process of (3-{[(RS)-1-(6-benzyl-3-chloro-2-methyl-7-oxo-6,7-dihydro-pyrazolo[1,5-c]pyrimidin-5-yl)-2-methyl-propyl]-[(4-trifluoromethyl-phenyl)-carbonyl]-amino}-propyl)-carbamic acid tert-butyl ester

There total 10 articles about (3-{[(RS)-1-(6-benzyl-3-chloro-2-methyl-7-oxo-6,7-dihydro-pyrazolo[1,5-c]pyrimidin-5-yl)-2-methyl-propyl]-[(4-trifluoromethyl-phenyl)-carbonyl]-amino}-propyl)-carbamic acid tert-butyl ester 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: 38.0%

: 960292-44-8
{3-[(RS)-1-(6-benzyl-3-chloro-2-methyl-7-oxo-6,7-dihydro-pyrazolo[1,5-c]pyrimidin-5-yl)-2-methyl-propylamino]-propyl}-carbamic acid tert-butyl ester

: 329-15-7
4-trifluoromethyl-phenyl acetyl chloride

: 960292-17-5
(3-{[(RS)-1-(6-benzyl-3-chloro-2-methyl-7-oxo-6,7-dihydro-pyrazolo[1,5-c]pyrimidin-5-yl)-2-methyl-propyl]-[(4-trifluoromethyl-phenyl)-carbonyl]-amino}-propyl)-carbamic acid tert-butyl ester

Guidance literature:: With pyridine; dmap; at 70 ℃; for 16h;

Reference yield:

: 960292-68-6
6-benzyl-3-chloro-2-methyl-7-oxo-6,7-dihydro-pyrazolo[1,5-c]pyrimidine-5-carbaldehyde

: 960292-17-5
(3-{[(RS)-1-(6-benzyl-3-chloro-2-methyl-7-oxo-6,7-dihydro-pyrazolo[1,5-c]pyrimidin-5-yl)-2-methyl-propyl]-[(4-trifluoromethyl-phenyl)-carbonyl]-amino}-propyl)-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: methyllithium / tetrahydrofuran; diethyl ether / 1 h / -78 °C

1.2: 2 h

2.1: 4-methylmorpholine N-oxide / dichloromethane / 0.5 h / 20 °C / Molecular sieve

2.2: 16 h / 20 °C

3.1: titanium(IV) isopropylate / tetrahydrofuran / 72 h / Heating / reflux

4.1: sodium tetrahydroborate; acetic acid / 1 h / 20 °C

5.1: pyridine / dmap / 16 h / 70 °C

With pyridine; titanium(IV) isopropylate; sodium tetrahydroborate; methyllithium; acetic acid; 4-methylmorpholine N-oxide; dmap; In tetrahydrofuran; diethyl ether; dichloromethane;

Reference yield:

: 626-53-9
1,3-diacetyl acetone

: 960292-17-5
(3-{[(RS)-1-(6-benzyl-3-chloro-2-methyl-7-oxo-6,7-dihydro-pyrazolo[1,5-c]pyrimidin-5-yl)-2-methyl-propyl]-[(4-trifluoromethyl-phenyl)-carbonyl]-amino}-propyl)-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 9 steps

1.1: sodium carbonate / water / 1 h / 100 °C

2.1: potassium carbonate / N,N-dimethyl-formamide / 14 h / 20 °C

3.1: N-chloro-succinimide / tetrachloromethane / 5 h / Heating / reflux

4.1: selenium(IV) oxide / 1,4-dioxane / 5 h / Heating / reflux

5.1: methyllithium / tetrahydrofuran; diethyl ether / 1 h / -78 °C

5.2: 2 h

6.1: 4-methylmorpholine N-oxide / dichloromethane / 0.5 h / 20 °C / Molecular sieve

6.2: 16 h / 20 °C

7.1: titanium(IV) isopropylate / tetrahydrofuran / 72 h / Heating / reflux

8.1: sodium tetrahydroborate; acetic acid / 1 h / 20 °C

9.1: pyridine / dmap / 16 h / 70 °C

With pyridine; titanium(IV) isopropylate; selenium(IV) oxide; sodium tetrahydroborate; N-chloro-succinimide; methyllithium; sodium carbonate; potassium carbonate; acetic acid; 4-methylmorpholine N-oxide; dmap; In tetrahydrofuran; 1,4-dioxane; tetrachloromethane; diethyl ether; dichloromethane; water; N,N-dimethyl-formamide;