(S)-2-(dimethylamino)-1-phenylethyl 6,6-dimethyl-3-(1-(trifluoromethyl)cyclobutanecarboxamido)-4,6 dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylate

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Chemical Name:(S)-2-(dimethylamino)-1-phenylethyl 6,6-dimethyl-3-(1-(trifluoromethyl)cyclobutanecarboxamido)-4,6 dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylate
CAS No.:1375799-72-6
Molecular Formula:C₂₄H₃₀F₃N₅O₃
Molecular Weight:493.529
Hs Code.:

(S)-2-(dimethylamino)-1-phenylethyl 6,6-dimethyl-3-(1-(trifluoromethyl)cyclobutanecarboxamido)-4,6 dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylate

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Chemical Property of (S)-2-(dimethylamino)-1-phenylethyl 6,6-dimethyl-3-(1-(trifluoromethyl)cyclobutanecarboxamido)-4,6 dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylate

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Technology Process of (S)-2-(dimethylamino)-1-phenylethyl 6,6-dimethyl-3-(1-(trifluoromethyl)cyclobutanecarboxamido)-4,6 dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylate

There total 3 articles about (S)-2-(dimethylamino)-1-phenylethyl 6,6-dimethyl-3-(1-(trifluoromethyl)cyclobutanecarboxamido)-4,6 dihydropyrrolo[3,4-c]pyrazole-5(1H)-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:

: C₂₇H₃₄F₃N₅O₅

: 1375799-72-6
(S)-2-(dimethylamino)-1-phenylethyl 6,6-dimethyl-3-(1-(trifluoromethyl)cyclobutanecarboxamido)-4,6 dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylate

Guidance literature:: With triethylamine; In methanol; at 20 ℃;
DOI:10.1021/jm300204j

Reference yield:

: 56613-81-1,1936-63-6
(S)-2-Amino-1-phenyl-1-ethanol

: 1375799-72-6
(S)-2-(dimethylamino)-1-phenylethyl 6,6-dimethyl-3-(1-(trifluoromethyl)cyclobutanecarboxamido)-4,6 dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: formic acid; water / 19 h / 20 - 95 °C

2: potassium carbonate / 1,2-dimethoxyethane / 80 °C

3: triethylamine / methanol / 20 °C

With potassium carbonate; triethylamine; In methanol; 1,2-dimethoxyethane; formic acid; water;
DOI:10.1021/jm300204j

Reference yield:

: 1375799-77-1
ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-(1-(trifluoromethyl)cyclobutanecarboxamido)-5,6-dihydropyrrolo[3,4-c]pyrazole-1(4H)-carboxylate

: 2202-68-8,2202-69-9,6853-14-1,34469-09-5
(S)-2-dimethylamino-1-phenylethanol

: 1375799-72-6
(S)-2-(dimethylamino)-1-phenylethyl 6,6-dimethyl-3-(1-(trifluoromethyl)cyclobutanecarboxamido)-4,6 dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / 1,2-dimethoxyethane / 80 °C

2: triethylamine / methanol / 20 °C

With potassium carbonate; triethylamine; In methanol; 1,2-dimethoxyethane;
DOI:10.1021/jm300204j