4-(Benzyloxy)-1-(1,2,3,4-tetrahydrobenzofuro[3,2-c]pyridin-7-yl)pyridin-2(1H)-one hydrochloride

Base Information

Chemical Name:4-(Benzyloxy)-1-(1,2,3,4-tetrahydrobenzofuro[3,2-c]pyridin-7-yl)pyridin-2(1H)-one hydrochloride
CAS No.:1613397-93-5
Molecular Formula:C₂₃H₂₀N₂O₃*ClH
Molecular Weight:408.884
Hs Code.:

Synonyms:4-(Benzyloxy)-1-(1,2,3,4-tetrahydrobenzofuro[3,2-c]pyridin-7-yl)pyridin-2(1H)-one hydrochloride

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Chemical Property of 4-(Benzyloxy)-1-(1,2,3,4-tetrahydrobenzofuro[3,2-c]pyridin-7-yl)pyridin-2(1H)-one hydrochloride

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Technology Process of 4-(Benzyloxy)-1-(1,2,3,4-tetrahydrobenzofuro[3,2-c]pyridin-7-yl)pyridin-2(1H)-one hydrochloride

There total 8 articles about 4-(Benzyloxy)-1-(1,2,3,4-tetrahydrobenzofuro[3,2-c]pyridin-7-yl)pyridin-2(1H)-one hydrochloride 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: 99.0%

: 1613399-49-7
4-(benzyloxy)-1-(1,2,3,4-tetrahydrobenzofuro[3,2-c]pyridin-7-yl)pyridin-2(1H)-one

: 1613397-93-5
4-(Benzyloxy)-1-(1,2,3,4-tetrahydrobenzofuro[3,2-c]pyridin-7-yl)pyridin-2(1H)-one hydrochloride

Guidance literature:: With hydrogenchloride; In diethyl ether;

Reference yield:

: 1613400-73-9
tert-butyl 7-(4-(benzyloxy)-2-oxopyridin-1(2H)-yl)-3,4-dihydrobenzofuro[3,2-c]pyridine-2(1H)-carboxylate

: 1613397-93-5
4-(Benzyloxy)-1-(1,2,3,4-tetrahydrobenzofuro[3,2-c]pyridin-7-yl)pyridin-2(1H)-one hydrochloride

Guidance literature:: With hydrogenchloride; In methanol; ethyl acetate; at 20 ℃; for 1h;
DOI:10.1002/cmdc.202100707

Reference yield:

: 1073-06-9
3-fluorobromobenzene

: 1613397-93-5
4-(Benzyloxy)-1-(1,2,3,4-tetrahydrobenzofuro[3,2-c]pyridin-7-yl)pyridin-2(1H)-one hydrochloride

Guidance literature:: Multi-step reaction with 6 steps

1.1: potassium tert-butylate / N,N-dimethyl-formamide / 0.5 h / 0 °C / Inert atmosphere

1.2: 2 h / 80 °C / Inert atmosphere

2.1: water; perchloric acid / 1,4-dioxane / 2 h / 20 °C

3.1: hydrogenchloride / isopropyl alcohol / Reflux

4.1: dichloromethane / 20 °C

5.1: caesium carbonate / toluene / 0.25 h / 20 °C / Inert atmosphere

5.2: 24 h / Inert atmosphere; Sealed tube; Reflux

6.1: hydrogenchloride / ethyl acetate; methanol / 1 h / 20 °C

With hydrogenchloride; perchloric acid; potassium tert-butylate; water; caesium carbonate; In 1,4-dioxane; methanol; dichloromethane; ethyl acetate; N,N-dimethyl-formamide; isopropyl alcohol; toluene;
DOI:10.1002/cmdc.202100707