tert-butyl 4-[4-(2-chloro-4-mesylbenzoyl)-5-fluoropyrrolo[2,3-d]pyrimidin-7-yl]piperidine-1-carboxylate

Base Information

Chemical Name:tert-butyl 4-[4-(2-chloro-4-mesylbenzoyl)-5-fluoropyrrolo[2,3-d]pyrimidin-7-yl]piperidine-1-carboxylate
CAS No.:1236281-81-4
Molecular Formula:C₂₄H₂₆ClFN₄O₅S
Molecular Weight:537.012
Hs Code.:

Synonyms:tert-butyl 4-[4-(2-chloro-4-mesylbenzoyl)-5-fluoropyrrolo[2,3-d]pyrimidin-7-yl]piperidine-1-carboxylate

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Chemical Property of tert-butyl 4-[4-(2-chloro-4-mesylbenzoyl)-5-fluoropyrrolo[2,3-d]pyrimidin-7-yl]piperidine-1-carboxylate

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Technology Process of tert-butyl 4-[4-(2-chloro-4-mesylbenzoyl)-5-fluoropyrrolo[2,3-d]pyrimidin-7-yl]piperidine-1-carboxylate

There total 3 articles about tert-butyl 4-[4-(2-chloro-4-mesylbenzoyl)-5-fluoropyrrolo[2,3-d]pyrimidin-7-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: 7.0%

: 1236284-39-1
tert-butyl 4-(4-chloro-5-fluoropyrrolo[2,3-d]pyrimidin-7-yl)piperidine-1-carboxylate

: 101349-95-5
2-chloro-4-(methylsulfonyl)benzaldehyde

: 1236281-81-4
tert-butyl 4-[4-(2-chloro-4-mesylbenzoyl)-5-fluoropyrrolo[2,3-d]pyrimidin-7-yl]piperidine-1-carboxylate

Guidance literature:: tert-butyl 4-(4-chloro-5-fluoropyrrolo[2,3-d]pyrimidin-7-yl)piperidine-1-carboxylate; 2-chloro-4-(methylsulfonyl)benzaldehyde; With sodium hydride; 1,3-dimethylimidazolim iodide; In 1,4-dioxane; mineral oil; at 20 ℃;

With ammonium chloride; In 1,4-dioxane; water; mineral oil;

Reference yield:

: 582313-57-3
4-chloro-7-fluoro-7-deazapurine

: 1236281-81-4
tert-butyl 4-[4-(2-chloro-4-mesylbenzoyl)-5-fluoropyrrolo[2,3-d]pyrimidin-7-yl]piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: triphenylphosphine; diethylazodicarboxylate / toluene; tetrahydrofuran / 1 h / 20 °C / Inert atmosphere

2: sodium hydride; 1,3-dimethylimidazolim iodide / 1,4-dioxane; mineral oil / 20 °C

With sodium hydride; 1,3-dimethylimidazolim iodide; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; 1,4-dioxane; toluene; mineral oil;

Reference yield:

: 3680-69-1
4-chloro-1H-pyrrolo[2,3-d]pyrimidine

: 1236281-81-4
tert-butyl 4-[4-(2-chloro-4-mesylbenzoyl)-5-fluoropyrrolo[2,3-d]pyrimidin-7-yl]piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: Selectfluor; acetic acid / acetonitrile / 18 h / 70 °C / Inert atmosphere

2: triphenylphosphine; diethylazodicarboxylate / toluene; tetrahydrofuran / 1 h / 20 °C / Inert atmosphere

3: sodium hydride; 1,3-dimethylimidazolim iodide / 1,4-dioxane; mineral oil / 20 °C

With sodium hydride; 1,3-dimethylimidazolim iodide; acetic acid; Selectfluor; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; 1,4-dioxane; toluene; acetonitrile; mineral oil;