5-(2-acetylaminopyrimidin-4-yl)-4-methoxy-9-tosylaminopyrido[3',2':4,5]pyrrolo[1,2-c]pyrimidine

Base Information

Chemical Name:5-(2-acetylaminopyrimidin-4-yl)-4-methoxy-9-tosylaminopyrido[3',2':4,5]pyrrolo[1,2-c]pyrimidine
CAS No.:397247-89-1
Molecular Formula:C₂₄H₂₁N₇O₄S
Molecular Weight:503.541
Hs Code.:

Synonyms:5-(2-acetylaminopyrimidin-4-yl)-4-methoxy-9-tosylaminopyrido[3',2':4,5]pyrrolo[1,2-c]pyrimidine

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Chemical Property of 5-(2-acetylaminopyrimidin-4-yl)-4-methoxy-9-tosylaminopyrido[3',2':4,5]pyrrolo[1,2-c]pyrimidine

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Technology Process of 5-(2-acetylaminopyrimidin-4-yl)-4-methoxy-9-tosylaminopyrido[3',2':4,5]pyrrolo[1,2-c]pyrimidine

There total 9 articles about 5-(2-acetylaminopyrimidin-4-yl)-4-methoxy-9-tosylaminopyrido[3',2':4,5]pyrrolo[1,2-c]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: 71.0%

: 397247-92-6
2-acetylamino-4-trimethylstannylpyrimidine

: 397247-88-0
5-iodo-4-methoxy-9-tosylaminopyrido[3',2':4,5]pyrrolo[1,2-c]pyrimidine

: 397247-89-1
5-(2-acetylaminopyrimidin-4-yl)-4-methoxy-9-tosylaminopyrido[3',2':4,5]pyrrolo[1,2-c]pyrimidine

Guidance literature:: With tris(dibenzylideneacetone)dipalladium ⁽⁰⁾; triphenylphosphine; lithium chloride; copper(l) iodide; In 1,4-dioxane; for 1h; Heating;
DOI:10.1021/jo035332b

Reference yield: 28.0%

: 397247-89-1
5-(2-acetylaminopyrimidin-4-yl)-4-methoxy-9-tosylaminopyrido[3',2':4,5]pyrrolo[1,2-c]pyrimidine

Guidance literature:

Reference yield:

: 122379-63-9
4-methoxy-1H-pyrrolo<2,3-b>pyridine

: 397247-89-1
5-(2-acetylaminopyrimidin-4-yl)-4-methoxy-9-tosylaminopyrido[3',2':4,5]pyrrolo[1,2-c]pyrimidine

Guidance literature:: Multi-step reaction with 8 steps

1.1: n-BuLi / tetrahydrofuran; hexane / 0.17 h / -78 °C

1.2: CO₂ / tetrahydrofuran; hexane / 0.67 h / -78 °C

1.3: 43 percent / t-BuLi / tetrahydrofuran; hexane / 1.83 h / -78 - 20 °C

2.1: 65 percent / hydrochloric acid / CHCl₃; benzene / 7 h / Heating

3.1: 95 percent / NH₂NH₂*H₂O / ethanol / 3 h / Heating

4.1: 65 percent / DIPEA / CH₂Cl₂ / 0.5 h

5.1: 80 percent / aq. HCl / CH₂Cl₂ / 1.5 h

6.1: 78 percent / TEA; MsCl / CH₂Cl₂ / 0.5 h / 0 °C

7.1: 95 percent / N-iodosuccinimide / CH₂Cl₂ / 0.08 h / -30 °C

8.1: 71 percent / Pd₂(dba)3; PPh₃; LiCl / CuI / dioxane / 1 h / Heating

With hydrogenchloride; N-iodo-succinimide; n-butyllithium; tris(dibenzylideneacetone)dipalladium ⁽⁰⁾; TEA; hydrazine hydrate; methanesulfonyl chloride; N-ethyl-N,N-diisopropylamine; triphenylphosphine; lithium chloride; copper(l) iodide; In tetrahydrofuran; 1,4-dioxane; ethanol; hexane; dichloromethane; chloroform; benzene;
DOI:10.1021/jo035332b