(R)-2-fluoro-4-[(5-{[[1-(7-hydroxynaphthalen-1-yl)-2-oxopyrrolidin-3-yl]amino]methyl}imidazol-1-yl)methyl]benzonitrile

Base Information

Chemical Name:(R)-2-fluoro-4-[(5-{[[1-(7-hydroxynaphthalen-1-yl)-2-oxopyrrolidin-3-yl]amino]methyl}imidazol-1-yl)methyl]benzonitrile
CAS No.:330186-32-8
Molecular Formula:C₂₆H₂₂FN₅O₂
Molecular Weight:455.491
Hs Code.:

Synonyms:(R)-2-fluoro-4-[(5-{[[1-(7-hydroxynaphthalen-1-yl)-2-oxopyrrolidin-3-yl]amino]methyl}imidazol-1-yl)methyl]benzonitrile

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Chemical Property of (R)-2-fluoro-4-[(5-{[[1-(7-hydroxynaphthalen-1-yl)-2-oxopyrrolidin-3-yl]amino]methyl}imidazol-1-yl)methyl]benzonitrile

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Technology Process of (R)-2-fluoro-4-[(5-{[[1-(7-hydroxynaphthalen-1-yl)-2-oxopyrrolidin-3-yl]amino]methyl}imidazol-1-yl)methyl]benzonitrile

There total 8 articles about (R)-2-fluoro-4-[(5-{[[1-(7-hydroxynaphthalen-1-yl)-2-oxopyrrolidin-3-yl]amino]methyl}imidazol-1-yl)methyl]benzonitrile 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:

: 2-Fluoro-4-(5-{[(Z)-(R)-1-(7-hydroxy-naphthalen-1-yl)-2-oxo-pyrrolidin-3-ylimino]-methyl}-imidazol-1-ylmethyl)-benzonitrile

: 330186-32-8
(R)-2-fluoro-4-[(5-{[[1-(7-hydroxynaphthalen-1-yl)-2-oxopyrrolidin-3-yl]amino]methyl}imidazol-1-yl)methyl]benzonitrile

Guidance literature:: With sodium cyanoborohydride; In methanol; at 20 ℃;
DOI:10.1021/jm010531d

Reference yield:

: 118-46-7
8-amino-2-naphthol

: 330186-32-8
(R)-2-fluoro-4-[(5-{[[1-(7-hydroxynaphthalen-1-yl)-2-oxopyrrolidin-3-yl]amino]methyl}imidazol-1-yl)methyl]benzonitrile

Guidance literature:: Multi-step reaction with 9 steps

1: 94 percent / CH₂Cl₂; tetrahydrofuran / 36 h / Heating

2: 97 percent / imidazole / dimethylformamide / 0.5 h / 20 °C

3: 95 percent / HCl(gas) / ethyl acetate / 0.5 h / 20 °C

4: PyBOP; DIEA / CH₂Cl₂

5: LiN(SiMe₃)2 / tetrahydrofuran / 0 °C

6: HCl(gas) / ethyl acetate / 0 °C

7: DIEA / methanol / 20 °C / pH 5

8: NaCNBH₃ / methanol / 20 °C

With 1H-imidazole; hydrogenchloride; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; sodium cyanoborohydride; N-ethyl-N,N-diisopropylamine; lithium hexamethyldisilazane; In tetrahydrofuran; methanol; dichloromethane; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1021/jm010531d

Reference yield:

: 301548-32-3
t-butyl (7-hydroxynaphthalen-1-yl)carbamate

: 330186-32-8
(R)-2-fluoro-4-[(5-{[[1-(7-hydroxynaphthalen-1-yl)-2-oxopyrrolidin-3-yl]amino]methyl}imidazol-1-yl)methyl]benzonitrile

Guidance literature:: Multi-step reaction with 8 steps

1: 97 percent / imidazole / dimethylformamide / 0.5 h / 20 °C

2: 95 percent / HCl(gas) / ethyl acetate / 0.5 h / 20 °C

3: PyBOP; DIEA / CH₂Cl₂

4: LiN(SiMe₃)2 / tetrahydrofuran / 0 °C

5: HCl(gas) / ethyl acetate / 0 °C

6: DIEA / methanol / 20 °C / pH 5

7: NaCNBH₃ / methanol / 20 °C

With 1H-imidazole; hydrogenchloride; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; sodium cyanoborohydride; N-ethyl-N,N-diisopropylamine; lithium hexamethyldisilazane; In tetrahydrofuran; methanol; dichloromethane; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1021/jm010531d