2-(3-methoxy-5-nitrophenyl)-4-(morpholin-4-yl)pyrido[3',2':4,5]furo[3,2-d]pyrimidine

Base Information

Chemical Name:2-(3-methoxy-5-nitrophenyl)-4-(morpholin-4-yl)pyrido[3',2':4,5]furo[3,2-d]pyrimidine
CAS No.:1509920-01-7
Molecular Formula:C₂₀H₁₇N₅O₅
Molecular Weight:407.385
Hs Code.:

Synonyms:2-(3-methoxy-5-nitrophenyl)-4-(morpholin-4-yl)pyrido[3',2':4,5]furo[3,2-d]pyrimidine

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Chemical Property of 2-(3-methoxy-5-nitrophenyl)-4-(morpholin-4-yl)pyrido[3',2':4,5]furo[3,2-d]pyrimidine

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Technology Process of 2-(3-methoxy-5-nitrophenyl)-4-(morpholin-4-yl)pyrido[3',2':4,5]furo[3,2-d]pyrimidine

There total 10 articles about 2-(3-methoxy-5-nitrophenyl)-4-(morpholin-4-yl)pyrido[3',2':4,5]furo[3,2-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:

: 1509919-87-2
3-(3-methoxy-5-nitrobenzamido)furo[2,3-b]pyridine-2-carboxamide

: 1509920-01-7
2-(3-methoxy-5-nitrophenyl)-4-(morpholin-4-yl)pyrido[3',2':4,5]furo[3,2-d]pyrimidine

Guidance literature:: Multi-step reaction with 3 steps

1: sodium hydroxide / isopropyl alcohol / 4 h / Reflux

2: trichlorophosphate / 4 h / 110 °C / Cooling with ice

3: toluene / 4 h / 0 - 135 °C

With sodium hydroxide; trichlorophosphate; In isopropyl alcohol; toluene;
DOI:10.1021/ml400378e

Reference yield:

: 6602-54-6
2-chloro-3-pyridinecarbonitrile

: 1509920-01-7
2-(3-methoxy-5-nitrophenyl)-4-(morpholin-4-yl)pyrido[3',2':4,5]furo[3,2-d]pyrimidine

Guidance literature:: Multi-step reaction with 8 steps

1: 1,8-diazabicyclo[5.4.0]undec-7-ene / ethanol / 75 °C

2: pyridine / tetrahydrofuran / 0 - 20 °C

3: sodium hydroxide; water / ethanol / 20 °C

4: thionyl chloride / 6 h / Reflux

5: ammonium hydroxide / methanol / 6 h / 50 °C

6: sodium hydroxide / isopropyl alcohol / 4 h / Reflux

7: trichlorophosphate / 4 h / 110 °C / Cooling with ice

8: toluene / 4 h / 0 - 135 °C

With pyridine; ammonium hydroxide; thionyl chloride; water; 1,8-diazabicyclo[5.4.0]undec-7-ene; sodium hydroxide; trichlorophosphate; In tetrahydrofuran; methanol; ethanol; isopropyl alcohol; toluene;
DOI:10.1021/ml400378e

Reference yield:

: 1509919-94-1
2-(3-methoxy-5-nitrophenyl)pyrido[3',2':4,5]furo[3,2-d]pyrimidin-4(3H)-one

: 1509920-01-7
2-(3-methoxy-5-nitrophenyl)-4-(morpholin-4-yl)pyrido[3',2':4,5]furo[3,2-d]pyrimidine

Guidance literature:: Multi-step reaction with 2 steps

1: trichlorophosphate / 4 h / 110 °C / Cooling with ice

2: toluene / 4 h / 0 - 135 °C

With trichlorophosphate; In toluene;
DOI:10.1021/ml400378e