(S)-3-(2-fluoro-4-(methylsulfonyl)phenylamino)-1-(1-(5-methoxypyrazin-2-yl)piperidin-4-yl)pyrrolidin-2-one

Base Information

Chemical Name:(S)-3-(2-fluoro-4-(methylsulfonyl)phenylamino)-1-(1-(5-methoxypyrazin-2-yl)piperidin-4-yl)pyrrolidin-2-one
CAS No.:1351167-70-8
Molecular Formula:C₂₁H₂₆FN₅O₄S
Molecular Weight:463.533
Hs Code.:

Synonyms:(S)-3-(2-fluoro-4-(methylsulfonyl)phenylamino)-1-(1-(5-methoxypyrazin-2-yl)piperidin-4-yl)pyrrolidin-2-one

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Chemical Property of (S)-3-(2-fluoro-4-(methylsulfonyl)phenylamino)-1-(1-(5-methoxypyrazin-2-yl)piperidin-4-yl)pyrrolidin-2-one

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Technology Process of (S)-3-(2-fluoro-4-(methylsulfonyl)phenylamino)-1-(1-(5-methoxypyrazin-2-yl)piperidin-4-yl)pyrrolidin-2-one

There total 6 articles about (S)-3-(2-fluoro-4-(methylsulfonyl)phenylamino)-1-(1-(5-methoxypyrazin-2-yl)piperidin-4-yl)pyrrolidin-2-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: 48.0%

: 143250-10-6
2-bromo-5-methoxypyrazine

: 1351167-86-6
(S)-3-(2-fluoro-4-(methylsulfonyl)phenylamino)-1-(piperidin-4-yl)pyrrolidin-2-one

: 1351167-70-8
(S)-3-(2-fluoro-4-(methylsulfonyl)phenylamino)-1-(1-(5-methoxypyrazin-2-yl)piperidin-4-yl)pyrrolidin-2-one

Guidance literature:: With sodium t-butanolate; palladium diacetate; DavePhos; In toluene; at 110 ℃; Inert atmosphere; Sealed tube;

Reference yield:

: 120278-07-1
benzyl 4-aminopiperidine-1-carboxylate

: 1351167-70-8
(S)-3-(2-fluoro-4-(methylsulfonyl)phenylamino)-1-(1-(5-methoxypyrazin-2-yl)piperidin-4-yl)pyrrolidin-2-one

Guidance literature:: Multi-step reaction with 7 steps

1.1: N-ethyl-N,N-diisopropylamine; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate / N,N-dimethyl-formamide / 0.5 h / 20 °C

1.2: 18 h / 20 °C

2.1: 4 h / 20 °C

3.1: lithium hexamethyldisilazane / tetrahydrofuran / 2 h / 0 - 20 °C

4.1: trifluoroacetic acid / dichloromethane / 1 h / 20 °C

5.1: sodium carbonate / dimethyl sulfoxide / 48 h / 120 °C

6.1: hydrogenchloride; hydrogen / palladium 10% on activated carbon / ethanol; water / 18 h / 2068.65 Torr

7.1: sodium t-butanolate / DavePhos; palladium diacetate / toluene / 110 °C / Inert atmosphere; Sealed tube

With hydrogenchloride; hydrogen; sodium carbonate; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; lithium hexamethyldisilazane; sodium t-butanolate; palladium 10% on activated carbon; palladium diacetate; DavePhos; In tetrahydrofuran; ethanol; dichloromethane; water; dimethyl sulfoxide; N,N-dimethyl-formamide; toluene;

Reference yield:

: 1351167-90-2
(S)-benzyl 4-(3-amino-2-oxopyrrolidin-1-yl)piperidin-1-carboxylate

: 1351167-70-8
(S)-3-(2-fluoro-4-(methylsulfonyl)phenylamino)-1-(1-(5-methoxypyrazin-2-yl)piperidin-4-yl)pyrrolidin-2-one

Guidance literature:: Multi-step reaction with 3 steps

1: sodium carbonate / dimethyl sulfoxide / 48 h / 120 °C

2: hydrogenchloride; hydrogen / palladium 10% on activated carbon / ethanol; water / 18 h / 2068.65 Torr

3: sodium t-butanolate / DavePhos; palladium diacetate / toluene / 110 °C / Inert atmosphere; Sealed tube

With hydrogenchloride; hydrogen; sodium carbonate; sodium t-butanolate; palladium 10% on activated carbon; palladium diacetate; DavePhos; In ethanol; water; dimethyl sulfoxide; toluene;