9-(4-chlorothiazol-2-yl)-1,3,8,8-tetramethyl-5-phenyl-8,9-dihydro-1H-pyrimido[4,5-a]pyrrolizine-2,4(3H,7H)-dione

Base Information

Chemical Name:9-(4-chlorothiazol-2-yl)-1,3,8,8-tetramethyl-5-phenyl-8,9-dihydro-1H-pyrimido[4,5-a]pyrrolizine-2,4(3H,7H)-dione
CAS No.:1614250-62-2
Molecular Formula:C₂₂H₂₁ClN₄O₂S
Molecular Weight:440.953
Hs Code.:

Synonyms:9-(4-chlorothiazol-2-yl)-1,3,8,8-tetramethyl-5-phenyl-8,9-dihydro-1H-pyrimido[4,5-a]pyrrolizine-2,4(3H,7H)-dione

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Chemical Property of 9-(4-chlorothiazol-2-yl)-1,3,8,8-tetramethyl-5-phenyl-8,9-dihydro-1H-pyrimido[4,5-a]pyrrolizine-2,4(3H,7H)-dione

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Technology Process of 9-(4-chlorothiazol-2-yl)-1,3,8,8-tetramethyl-5-phenyl-8,9-dihydro-1H-pyrimido[4,5-a]pyrrolizine-2,4(3H,7H)-dione

There total 9 articles about 9-(4-chlorothiazol-2-yl)-1,3,8,8-tetramethyl-5-phenyl-8,9-dihydro-1H-pyrimido[4,5-a]pyrrolizine-2,4(3H,7H)-dione 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:

: 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-dimethylpropyl methanesulfonate

: 1614250-62-2
9-(4-chlorothiazol-2-yl)-1,3,8,8-tetramethyl-5-phenyl-8,9-dihydro-1H-pyrimido[4,5-a]pyrrolizine-2,4(3H,7H)-dione

Guidance literature:: With sodium hydride; In tetrahydrofuran; at 20 ℃; for 0.0833333h;

Reference yield:

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

: 1614250-62-2
9-(4-chlorothiazol-2-yl)-1,3,8,8-tetramethyl-5-phenyl-8,9-dihydro-1H-pyrimido[4,5-a]pyrrolizine-2,4(3H,7H)-dione

Guidance literature:: Multi-step reaction with 6 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

4.1: sodium tetrahydroborate; methanol; lithium chloride / 0.5 h / 20 °C

5.1: triethylamine / dichloromethane / 0.08 h / 20 °C

6.1: sodium hydride / tetrahydrofuran / 0.08 h / 20 °C

With methanol; sodium tetrahydroborate; TurboGrignard; boron trifluoride-tetrahydrofuran complex; sodium hydride; triethylamine; lithium chloride; trichlorophosphate; In tetrahydrofuran; dichloromethane; 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

: 1614250-62-2
9-(4-chlorothiazol-2-yl)-1,3,8,8-tetramethyl-5-phenyl-8,9-dihydro-1H-pyrimido[4,5-a]pyrrolizine-2,4(3H,7H)-dione

Guidance literature:: Multi-step reaction with 5 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

3.1: sodium tetrahydroborate; methanol; lithium chloride / 0.5 h / 20 °C

4.1: triethylamine / dichloromethane / 0.08 h / 20 °C

5.1: sodium hydride / tetrahydrofuran / 0.08 h / 20 °C

With methanol; sodium tetrahydroborate; TurboGrignard; boron trifluoride-tetrahydrofuran complex; sodium hydride; triethylamine; lithium chloride; In tetrahydrofuran; dichloromethane;