6-bromo-4-(cyclopropylmethoxy)-2-(methylthio)-5-phenylfuro[2,3-d]pyrimidine

Base Information

Chemical Name:6-bromo-4-(cyclopropylmethoxy)-2-(methylthio)-5-phenylfuro[2,3-d]pyrimidine
CAS No.:1301612-14-5
Molecular Formula:C₁₇H₁₅BrN₂O₂S
Molecular Weight:391.288
Hs Code.:

Synonyms:6-bromo-4-(cyclopropylmethoxy)-2-(methylthio)-5-phenylfuro[2,3-d]pyrimidine

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Chemical Property of 6-bromo-4-(cyclopropylmethoxy)-2-(methylthio)-5-phenylfuro[2,3-d]pyrimidine

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Technology Process of 6-bromo-4-(cyclopropylmethoxy)-2-(methylthio)-5-phenylfuro[2,3-d]pyrimidine

There total 3 articles about 6-bromo-4-(cyclopropylmethoxy)-2-(methylthio)-5-phenylfuro[2,3-d]pyrimidine 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:

: 1301610-69-4
6-bromo-2-(methylthio)-5-phenylfuro[2,3-d]pyrimidin-4(3H)-one

: 7051-34-5
cyclopropylcarbinyl bromide

: 1301612-14-5
6-bromo-4-(cyclopropylmethoxy)-2-(methylthio)-5-phenylfuro[2,3-d]pyrimidine

: 1301612-12-3
6-bromo-3-(cyclopropylmethyl)-2-(methylthio)-5-phenylfuro[2,3-d]pyrimidin-4(3H)-one

Guidance literature:: With lithium hydroxide; In 1,4-dioxane; water; at 70 ℃;

Reference yield:

: 10428-49-6
β-chloro-β-nitrostyrene

: 1301612-14-5
6-bromo-4-(cyclopropylmethoxy)-2-(methylthio)-5-phenylfuro[2,3-d]pyrimidine

: 1301612-12-3
6-bromo-3-(cyclopropylmethyl)-2-(methylthio)-5-phenylfuro[2,3-d]pyrimidin-4(3H)-one

Guidance literature:: Multi-step reaction with 3 steps

1: 1,8-diazabicyclo[5.4.0]undec-7-ene / ethanol / 96 h / Inert atmosphere; Reflux

2: N-Bromosuccinimide; potassium acetate / N,N-dimethyl-formamide / 80 °C / Inert atmosphere; Sealed tube

3: lithium hydroxide / 1,4-dioxane; water / 70 °C

With N-Bromosuccinimide; potassium acetate; 1,8-diazabicyclo[5.4.0]undec-7-ene; lithium hydroxide; In 1,4-dioxane; ethanol; water; N,N-dimethyl-formamide;

Reference yield:

: 1979-98-2
2,4-dihydroxy-2-methylmercaptopyrimidine (hydroxy-keto form)

: 1301612-14-5
6-bromo-4-(cyclopropylmethoxy)-2-(methylthio)-5-phenylfuro[2,3-d]pyrimidine

: 1301612-12-3
6-bromo-3-(cyclopropylmethyl)-2-(methylthio)-5-phenylfuro[2,3-d]pyrimidin-4(3H)-one

Guidance literature:: Multi-step reaction with 3 steps

1: 1,8-diazabicyclo[5.4.0]undec-7-ene / ethanol / 96 h / Inert atmosphere; Reflux

2: N-Bromosuccinimide; potassium acetate / N,N-dimethyl-formamide / 80 °C / Inert atmosphere; Sealed tube

3: lithium hydroxide / 1,4-dioxane; water / 70 °C

With N-Bromosuccinimide; potassium acetate; 1,8-diazabicyclo[5.4.0]undec-7-ene; lithium hydroxide; In 1,4-dioxane; ethanol; water; N,N-dimethyl-formamide;