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2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenyl → (S)-3-(2-fluoro-4-(methylsulfonyl)phenylamino)-1-(1-(5-methoxypyrazin-2-yl)piperidin-4-yl)pyrrolidin-2-one

HRID 408017
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HRID 408017 반응식
[F:1][C:2]1[CH:7]=[C:6]([S:8]([CH3:11])(=[O:10])=[O:9])[CH:5]=[CH:4][C:3]=1[NH:12][C@H:13]1[CH2:17][CH2:16][N:15]([CH:18]2[CH2:23][CH2:22][NH:21][CH2:20][CH2:19]2)[C:14]1=[O:24].Br[C:26]1[CH:31]=[N:30][C:29]([O:32][CH3:33])=[CH:28][N:27]=1.CC([O-])(C)C.[Na+].C1(P(C2CCCCC2)C2C=CC=CC=2C2C=CC=CC=2N(C)C)CCCCC1>CC([O-])=O.CC([O-])=O.[Pd+2].C1(C)C=CC=CC=1>[F:1][C:2]1[CH:7]=[C:6]([S:8]([CH3:11])(=[O:10])=[O:9])[CH:5]=[CH:4][C:3]=1[NH:12][C@H:13]1[CH2:17][CH2:16][N:15]([CH:18]2[CH2:23][CH2:22][N:21]([C:26]3[CH:31]=[N:30][C:29]([O:32][CH3:33])=[CH:28][N:27]=3)[CH2:20][CH2:19]2)[C:14]1=[O:24]
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참가 물질

7

반응물 4

HCID 27342172-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 197561722-Bromo-5-methoxypyrazineHCID 23676156Sodium t-butoxideHCID 66800375(S)-3-(2-fluoro-4-(methylsulfonyl)phenylamino)-1-(piperidin-4-yl)pyrrolidin-2-one

생성물 1

HCID 54670619(S)-3-(2-fluoro-4-(methylsulfonyl)phenylamino)-1-(1-(5-methoxypyrazin-2-yl)piperidin-4-yl)pyrrolidin-2-one
수율 48%

시약·촉매·용매 2

HCID 167845palladium(II) acetate촉매HCID 1140Toluene용매

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온도
110 °C

실험 절차

(S)-3-(2-Fluoro-4-(methylsulfonyl)phenylamino)-1-(piperidin-4-yl)pyrrolidin-2-one (Preparation E; 0.050 g, 0.14 mmol), 2-bromo-5-methoxypyrazine (0.032 g, 0.17 mmol), NaOtBu (0.041 g, 0.42 mmol), Pd(OAc)2 (0.005 g, 0.02 mmol), and 2-dicyclohexylphosphino-2′-(N,N-dimethylamino)-biphenyl (DavePHOS) (0.017 g, 0.042 mmol) were added to an argon-filled sealable flask. Toluene (1.5 mL) was added and the mixture was purged with bubbling argon for 5 minutes. The vessel was sealed and the mixture was stirred at 110° C. overnight. The mixture was cooled to ambient temperature, diluted with THF (12 mL), and stirred for 15 minutes. The mixture was filtered through GF/F paper and concentrated. The residue was purified by silica chromatography (EtOAc) to afford (S)-3-(2-fluoro-4-(methylsulfonyl)phenylamino)-1-(1-(5-methoxypyrazin-2-yl)piperidin-4-yl)pyrrolidin-2-one (0.031 g, 0.067 mmol, 48% yield). Mass spectrum (apci) m/z=464.2 (M+H). Optical purity was not determined.

후처리

  1. additionfilled sealable flask
  2. customthe mixture was purged with bubbling argon for 5 minutes
  3. customThe vessel was sealed
  4. temperatureThe mixture was cooled to ambient temperature
  5. additiondiluted with THF (12 mL)
  6. stirringstirred for 15 minutes
  7. filtrationThe mixture was filtered through GF/F paper
  8. concentrationconcentrated
  9. customThe residue was purified by silica chromatography (EtOAc)

출처 및 근거

ORD 기록
ord-cf3780c86d0c473eb45c0bcf0e0365c6
출처 데이터셋
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08754226B2

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