(2-(5-fluoropyridin-3-yl)-4-hydroxy-1-oxa-9-azaspiro[5.5]undec-2-en-9-yl)-(4-isopropoxy-3-methylphenyl)methanone

Base Information

Chemical Name:(2-(5-fluoropyridin-3-yl)-4-hydroxy-1-oxa-9-azaspiro[5.5]undec-2-en-9-yl)-(4-isopropoxy-3-methylphenyl)methanone
CAS No.:1448520-32-8
Molecular Formula:C₂₅H₂₉FN₂O₄
Molecular Weight:440.515
Hs Code.:

Synonyms:(2-(5-fluoropyridin-3-yl)-4-hydroxy-1-oxa-9-azaspiro[5.5]undec-2-en-9-yl)-(4-isopropoxy-3-methylphenyl)methanone

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Chemical Property of (2-(5-fluoropyridin-3-yl)-4-hydroxy-1-oxa-9-azaspiro[5.5]undec-2-en-9-yl)-(4-isopropoxy-3-methylphenyl)methanone

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Technology Process of (2-(5-fluoropyridin-3-yl)-4-hydroxy-1-oxa-9-azaspiro[5.5]undec-2-en-9-yl)-(4-isopropoxy-3-methylphenyl)methanone

There total 5 articles about (2-(5-fluoropyridin-3-yl)-4-hydroxy-1-oxa-9-azaspiro[5.5]undec-2-en-9-yl)-(4-isopropoxy-3-methylphenyl)methanone 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:

: 1448520-31-7
2-(5-fluoropyridin-3-yl)-9-(4-isopropoxy-3-methylbenzoyl)-1-oxa-9-azaspiro[5.5]undec-2-en-4-one

: 1448520-32-8
(2-(5-fluoropyridin-3-yl)-4-hydroxy-1-oxa-9-azaspiro[5.5]undec-2-en-9-yl)-(4-isopropoxy-3-methylphenyl)methanone

Guidance literature:: With methanol; sodium tetrahydroborate; for 0.5h;

Reference yield:

: 1368442-54-9
1-(4-isopropoxy-3-methylbenzoyl)piperidin-4-one

: 1448520-32-8
(2-(5-fluoropyridin-3-yl)-4-hydroxy-1-oxa-9-azaspiro[5.5]undec-2-en-9-yl)-(4-isopropoxy-3-methylphenyl)methanone

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hydride / tetrahydrofuran; mineral oil / 0.5 h / 0 - 25 °C / Inert atmosphere

1.2: 24 h / 25 °C / Inert atmosphere

2.1: N-ethyl-N,N-diisopropylamine; t-butyldimethylsiyl triflate / dichloromethane / 0.5 h / 0 °C

2.2: 0.08 h / -78 °C

3.1: Dess-Martin periodane / dichloromethane / 1 h / 0 °C

4.1: acetic acid / 1 h / 120 °C

5.1: sodium tetrahydroborate; methanol / 0.5 h

With methanol; sodium tetrahydroborate; t-butyldimethylsiyl triflate; sodium hydride; Dess-Martin periodane; acetic acid; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; mineral oil;

Reference yield:

: 1448520-28-2
1-(1-(4-isopropoxy-3-methylbenzoyl)piperidin-4-ylidene)propan-2-one

: 1448520-32-8
(2-(5-fluoropyridin-3-yl)-4-hydroxy-1-oxa-9-azaspiro[5.5]undec-2-en-9-yl)-(4-isopropoxy-3-methylphenyl)methanone

Guidance literature:: Multi-step reaction with 4 steps

1.1: N-ethyl-N,N-diisopropylamine; t-butyldimethylsiyl triflate / dichloromethane / 0.5 h / 0 °C

1.2: 0.08 h / -78 °C

2.1: Dess-Martin periodane / dichloromethane / 1 h / 0 °C

3.1: acetic acid / 1 h / 120 °C

4.1: sodium tetrahydroborate; methanol / 0.5 h

With methanol; sodium tetrahydroborate; t-butyldimethylsiyl triflate; Dess-Martin periodane; acetic acid; N-ethyl-N,N-diisopropylamine; In dichloromethane;