(S)-4-(4-((2-hydroxy-1-phenylethyl)amino)-7H-pyrrolo[2,3-d]pyrimidin-6-yl)-3-methoxybenzaldehyde

Base Information

Chemical Name:(S)-4-(4-((2-hydroxy-1-phenylethyl)amino)-7H-pyrrolo[2,3-d]pyrimidin-6-yl)-3-methoxybenzaldehyde
CAS No.:1637438-04-0
Molecular Formula:C₂₂H₂₀N₄O₃
Molecular Weight:388.426
Hs Code.:

Synonyms:(S)-4-(4-((2-hydroxy-1-phenylethyl)amino)-7H-pyrrolo[2,3-d]pyrimidin-6-yl)-3-methoxybenzaldehyde

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Chemical Property of (S)-4-(4-((2-hydroxy-1-phenylethyl)amino)-7H-pyrrolo[2,3-d]pyrimidin-6-yl)-3-methoxybenzaldehyde

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Technology Process of (S)-4-(4-((2-hydroxy-1-phenylethyl)amino)-7H-pyrrolo[2,3-d]pyrimidin-6-yl)-3-methoxybenzaldehyde

There total 6 articles about (S)-4-(4-((2-hydroxy-1-phenylethyl)amino)-7H-pyrrolo[2,3-d]pyrimidin-6-yl)-3-methoxybenzaldehyde 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: 83.0%

: 1028479-47-1
(4-formyl-2-methoxyphenyl) boronic acid

: 1643962-38-2
(S)-2-((6-iodo-7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)-2-phenylethan-1-ol

: 1637438-04-0
(S)-4-(4-((2-hydroxy-1-phenylethyl)amino)-7H-pyrrolo[2,3-d]pyrimidin-6-yl)-3-methoxybenzaldehyde

Guidance literature:: With chloro(2-dicyclohexylphosphino-2’,4’,6’-triisopropyl-1,1‘-biphenyl)[2-(2’-amino-1,1‘-biphenyl’)]palladium(II); potassium carbonate; XPhos; In 1,4-dioxane; water; at 100 ℃; for 3h;

Reference yield:

: 3680-71-5
Allopurinol

: 1637438-04-0
(S)-4-(4-((2-hydroxy-1-phenylethyl)amino)-7H-pyrrolo[2,3-d]pyrimidin-6-yl)-3-methoxybenzaldehyde

Guidance literature:: Multi-step reaction with 6 steps

1.1: trichlorophosphate / Heating

2.1: sodium t-butanolate

3.1: lithium diisopropyl amide

3.2: -78 °C

4.1: methanol; sodium hydroxide

5.1: butan-1-ol / 145 °C

6.1: XPhos; potassium carbonate; (chloro(2-dicyclohexylphosphino-2′,4′,6′-triisopropyl-1,1′-biphenyl)[2-(2′-amino-1,1′-biphenyl)]palladium(II)) / 1,4-dioxane; water / 100 °C / Inert atmosphere

With methanol; (chloro(2-dicyclohexylphosphino-2′,4′,6′-triisopropyl-1,1′-biphenyl)[2-(2′-amino-1,1′-biphenyl)]palladium(II)); potassium carbonate; sodium hydroxide; sodium t-butanolate; lithium diisopropyl amide; XPhos; trichlorophosphate; In 1,4-dioxane; water; butan-1-ol; 6.1: |Suzuki Coupling;
DOI:10.1016/j.ejps.2014.04.011

Reference yield:

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

: 1637438-04-0
(S)-4-(4-((2-hydroxy-1-phenylethyl)amino)-7H-pyrrolo[2,3-d]pyrimidin-6-yl)-3-methoxybenzaldehyde

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium t-butanolate

2.1: lithium diisopropyl amide

2.2: -78 °C

3.1: methanol; sodium hydroxide

4.1: butan-1-ol / 145 °C

5.1: XPhos; potassium carbonate; (chloro(2-dicyclohexylphosphino-2′,4′,6′-triisopropyl-1,1′-biphenyl)[2-(2′-amino-1,1′-biphenyl)]palladium(II)) / 1,4-dioxane; water / 100 °C / Inert atmosphere

With methanol; (chloro(2-dicyclohexylphosphino-2′,4′,6′-triisopropyl-1,1′-biphenyl)[2-(2′-amino-1,1′-biphenyl)]palladium(II)); potassium carbonate; sodium hydroxide; sodium t-butanolate; lithium diisopropyl amide; XPhos; In 1,4-dioxane; water; butan-1-ol; 5.1: |Suzuki Coupling;
DOI:10.1016/j.ejps.2014.04.011