tert-butyl 4-(7-(1-ethoxy-2-methyl-1-oxo-3-phenylpropan-2-yl)pyrazolo[1,5-a]pyrimidin-3-yl)piperidine-1-carboxylate

Base Information

Chemical Name:tert-butyl 4-(7-(1-ethoxy-2-methyl-1-oxo-3-phenylpropan-2-yl)pyrazolo[1,5-a]pyrimidin-3-yl)piperidine-1-carboxylate
CAS No.:1264294-91-8
Molecular Formula:C₂₈H₃₆N₄O₄
Molecular Weight:492.618
Hs Code.:

Synonyms:tert-butyl 4-(7-(1-ethoxy-2-methyl-1-oxo-3-phenylpropan-2-yl)pyrazolo[1,5-a]pyrimidin-3-yl)piperidine-1-carboxylate

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Chemical Property of tert-butyl 4-(7-(1-ethoxy-2-methyl-1-oxo-3-phenylpropan-2-yl)pyrazolo[1,5-a]pyrimidin-3-yl)piperidine-1-carboxylate

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Technology Process of tert-butyl 4-(7-(1-ethoxy-2-methyl-1-oxo-3-phenylpropan-2-yl)pyrazolo[1,5-a]pyrimidin-3-yl)piperidine-1-carboxylate

There total 5 articles about tert-butyl 4-(7-(1-ethoxy-2-methyl-1-oxo-3-phenylpropan-2-yl)pyrazolo[1,5-a]pyrimidin-3-yl)piperidine-1-carboxylate 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:

: 1264296-05-0
ethyl 2-benzyl-5-(dimethylamino)-2-methyl-3-oxopent-4-enoate

: 1264296-09-4
tert-butyl 4-(5-amino-1H-pyrazol-4-yl)piperidine-1-carboxylate

: 1264294-91-8
tert-butyl 4-(7-(1-ethoxy-2-methyl-1-oxo-3-phenylpropan-2-yl)pyrazolo[1,5-a]pyrimidin-3-yl)piperidine-1-carboxylate

Guidance literature:: With trifluoroacetic acid; In ethanol; at 60 ℃; for 1h;

Reference yield:

: 256411-39-9
tert-butyl 4-(cyanomethyl)piperidine-1-carboxylate

: 1264294-91-8
tert-butyl 4-(7-(1-ethoxy-2-methyl-1-oxo-3-phenylpropan-2-yl)pyrazolo[1,5-a]pyrimidin-3-yl)piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: diisopropylamine; n-butyllithium / hexane; tetrahydrofuran / -78 °C

1.2: 0.5 h / Cooling with ice/water

2.1: hydrazine hydrate / ethanol; water / 2 h / 60 °C

3.1: trifluoroacetic acid / ethanol / 1 h / 60 °C

With n-butyllithium; hydrazine hydrate; diisopropylamine; trifluoroacetic acid; In tetrahydrofuran; ethanol; hexane; water;

Reference yield:

: 107449-78-5
ethyl α-methyl-α-benzylacetoacetate

: 1264294-91-8
tert-butyl 4-(7-(1-ethoxy-2-methyl-1-oxo-3-phenylpropan-2-yl)pyrazolo[1,5-a]pyrimidin-3-yl)piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: N,N-dimethyl-formamide / 90 °C

2: trifluoroacetic acid / ethanol / 1 h / 60 °C

With trifluoroacetic acid; In ethanol; N,N-dimethyl-formamide;