methyl 3-(4-chlorothiazol-2-yl)-3-(1,3-dimethyl-2,4-dioxo-5-phenyl-2,3,4,6-tetrahydro-1H-pyrrolo[3,4-d]pyrimidin-7-yl)-2,2-dimethylpropanoate

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Chemical Name:methyl 3-(4-chlorothiazol-2-yl)-3-(1,3-dimethyl-2,4-dioxo-5-phenyl-2,3,4,6-tetrahydro-1H-pyrrolo[3,4-d]pyrimidin-7-yl)-2,2-dimethylpropanoate
CAS No.:1614251-90-9
Molecular Formula:C₂₃H₂₃ClN₄O₄S
Molecular Weight:486.979
Hs Code.:

Synonyms:methyl 3-(4-chlorothiazol-2-yl)-3-(1,3-dimethyl-2,4-dioxo-5-phenyl-2,3,4,6-tetrahydro-1H-pyrrolo[3,4-d]pyrimidin-7-yl)-2,2-dimethylpropanoate

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Chemical Property of methyl 3-(4-chlorothiazol-2-yl)-3-(1,3-dimethyl-2,4-dioxo-5-phenyl-2,3,4,6-tetrahydro-1H-pyrrolo[3,4-d]pyrimidin-7-yl)-2,2-dimethylpropanoate

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Technology Process of methyl 3-(4-chlorothiazol-2-yl)-3-(1,3-dimethyl-2,4-dioxo-5-phenyl-2,3,4,6-tetrahydro-1H-pyrrolo[3,4-d]pyrimidin-7-yl)-2,2-dimethylpropanoate

There total 5 articles about methyl 3-(4-chlorothiazol-2-yl)-3-(1,3-dimethyl-2,4-dioxo-5-phenyl-2,3,4,6-tetrahydro-1H-pyrrolo[3,4-d]pyrimidin-7-yl)-2,2-dimethylpropanoate 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:

: 924840-49-3
1,3-dimethyl-5-phenyl-1H-pyrrolo[3,4-d]pyrimidine-2,4(3H,6H)-dione

: 1614251-90-9
methyl 3-(4-chlorothiazol-2-yl)-3-(1,3-dimethyl-2,4-dioxo-5-phenyl-2,3,4,6-tetrahydro-1H-pyrrolo[3,4-d]pyrimidin-7-yl)-2,2-dimethylpropanoate

Guidance literature:: Multi-step reaction with 3 steps

1.1: trichlorophosphate / N,N-dimethyl-formamide / 0.25 h / 0 °C

2.1: TurboGrignard / tetrahydrofuran / 0.08 h / 0 °C

2.2: 0.25 h / 0 °C

3.1: boron trifluoride-tetrahydrofuran complex / tetrahydrofuran / 0.08 h / 20 °C

With TurboGrignard; boron trifluoride-tetrahydrofuran complex; trichlorophosphate; In tetrahydrofuran; N,N-dimethyl-formamide;

Reference yield:

: 1614252-63-9
1,3-dimethyl-2,4-dioxo-5-phenyl-2,3,4,6-tetrahydro-1H-pyrrolo[3,4-d]pyrimidine-7-carbaldehyde

: 1614251-90-9
methyl 3-(4-chlorothiazol-2-yl)-3-(1,3-dimethyl-2,4-dioxo-5-phenyl-2,3,4,6-tetrahydro-1H-pyrrolo[3,4-d]pyrimidin-7-yl)-2,2-dimethylpropanoate

Guidance literature:: Multi-step reaction with 2 steps

1.1: TurboGrignard / tetrahydrofuran / 0.08 h / 0 °C

1.2: 0.25 h / 0 °C

2.1: boron trifluoride-tetrahydrofuran complex / tetrahydrofuran / 0.08 h / 20 °C

With TurboGrignard; boron trifluoride-tetrahydrofuran complex; In tetrahydrofuran;

Reference yield:

: 443667-38-7
5-benzoyl-6-(bromomethyl)-1,3-dimethylpyrimidine-2,4(1H,3H)-dione

: 1614251-90-9
methyl 3-(4-chlorothiazol-2-yl)-3-(1,3-dimethyl-2,4-dioxo-5-phenyl-2,3,4,6-tetrahydro-1H-pyrrolo[3,4-d]pyrimidin-7-yl)-2,2-dimethylpropanoate

Guidance literature:: Multi-step reaction with 4 steps

1.1: triethylamine; 1,1,1,3,3,3-hexamethyl-disilazane / 1,4-dioxane / 22 h / Reflux

2.1: trichlorophosphate / N,N-dimethyl-formamide / 0.25 h / 0 °C

3.1: TurboGrignard / tetrahydrofuran / 0.08 h / 0 °C

3.2: 0.25 h / 0 °C

4.1: boron trifluoride-tetrahydrofuran complex / tetrahydrofuran / 0.08 h / 20 °C

With TurboGrignard; boron trifluoride-tetrahydrofuran complex; triethylamine; 1,1,1,3,3,3-hexamethyl-disilazane; trichlorophosphate; In tetrahydrofuran; 1,4-dioxane; N,N-dimethyl-formamide;