3-(4-fluorophenyl)-3-isobutyl-5-(3-(piperidin-1-yl)propanoyl)-4,5,6,7-tetrahydrofuro[3,4-c]pyridin-1(3H)-one

Base Information

Chemical Name:3-(4-fluorophenyl)-3-isobutyl-5-(3-(piperidin-1-yl)propanoyl)-4,5,6,7-tetrahydrofuro[3,4-c]pyridin-1(3H)-one
CAS No.:1443250-89-2
Molecular Formula:C₂₅H₃₃FN₂O₃
Molecular Weight:428.547
Hs Code.:

Synonyms:3-(4-fluorophenyl)-3-isobutyl-5-(3-(piperidin-1-yl)propanoyl)-4,5,6,7-tetrahydrofuro[3,4-c]pyridin-1(3H)-one

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Chemical Property of 3-(4-fluorophenyl)-3-isobutyl-5-(3-(piperidin-1-yl)propanoyl)-4,5,6,7-tetrahydrofuro[3,4-c]pyridin-1(3H)-one

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Technology Process of 3-(4-fluorophenyl)-3-isobutyl-5-(3-(piperidin-1-yl)propanoyl)-4,5,6,7-tetrahydrofuro[3,4-c]pyridin-1(3H)-one

There total 4 articles about 3-(4-fluorophenyl)-3-isobutyl-5-(3-(piperidin-1-yl)propanoyl)-4,5,6,7-tetrahydrofuro[3,4-c]pyridin-1(3H)-one 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: 27.0%

: 26371-07-3
1-piperidinepropionic acid

: 1443251-49-7
3-(4-fluorophenyl)-3-isobutyl-4,5,6,7-tetrahydrofuro[3,4-c]pyridin-1(3H)-one

: 1443250-89-2
3-(4-fluorophenyl)-3-isobutyl-5-(3-(piperidin-1-yl)propanoyl)-4,5,6,7-tetrahydrofuro[3,4-c]pyridin-1(3H)-one

Guidance literature:: With (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; at 20 ℃; for 16h;

Reference yield:

: 1194-02-1,143234-87-1
4-fluorobenzonitrile

: 1443250-89-2
3-(4-fluorophenyl)-3-isobutyl-5-(3-(piperidin-1-yl)propanoyl)-4,5,6,7-tetrahydrofuro[3,4-c]pyridin-1(3H)-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: diethyl ether; tetrahydrofuran / 16 h / Reflux

1.2: 0.5 h / 0 °C

2.1: lithium diisopropyl amide / diethyl ether / 2 h / -78 °C

2.2: 0.5 h / -78 °C

2.3: 12 h

3.1: hydrogenchloride / diethyl ether; dichloromethane / 0.67 h / 0 °C

3.2: 0.5 h / 2068.65 Torr

4.1: N-ethyl-N,N-diisopropylamine; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate / tetrahydrofuran / 16 h / 20 °C

With hydrogenchloride; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; lithium diisopropyl amide; In tetrahydrofuran; diethyl ether; dichloromethane;

Reference yield:

: 1443251-48-6
3-(4-fluorophenyl)-3-isobutylfuro[3,4-c]pyridin-1(3H)-one

: 1443250-89-2
3-(4-fluorophenyl)-3-isobutyl-5-(3-(piperidin-1-yl)propanoyl)-4,5,6,7-tetrahydrofuro[3,4-c]pyridin-1(3H)-one

Guidance literature:: Multi-step reaction with 2 steps

1.1: hydrogenchloride / diethyl ether; dichloromethane / 0.67 h / 0 °C

1.2: 0.5 h / 2068.65 Torr

2.1: N-ethyl-N,N-diisopropylamine; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate / tetrahydrofuran / 16 h / 20 °C

With hydrogenchloride; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; diethyl ether; dichloromethane;