Bromoacetonitrile → 6-Chloro-N-(cyanomethyl)-N-{(3S)-1-[(1S)-1-methyl-2-oxo-2-piperidin-1-ylethyl]-2-oxopyrrolidin-3-yl}naphthalene-2-sulfonamide

HRID 7315

반응식

HRID 7315 반응식
[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[CH:8]=[C:7]([S:12]([NH:15][C@H:16]1[CH2:20][CH2:19][N:18]([C@@H:21]([CH3:30])[C:22](=[O:29])[N:23]3[CH2:28][CH2:27][CH2:26][CH2:25][CH2:24]3)[C:17]1=[O:31])(=[O:14])=[O:13])[CH:6]=[CH:5]2.C[Si]([N-][Si](C)(C)C)(C)C.[Li+].Br[CH2:43][C:44]#[N:45]>C1COCC1>[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[CH:8]=[C:7]([S:12]([N:15]([CH2:43][C:44]#[N:45])[C@H:16]1[CH2:20][CH2:19][N:18]([C@@H:21]([CH3:30])[C:22](=[O:29])[N:23]3[CH2:28][CH2:27][CH2:26][CH2:25][CH2:24]3)[C:17]1=[O:31])(=[O:13])=[O:14])[CH:6]=[CH:5]2

참가 물질

5

반응물 3

HCID 11534BromoacetonitrileHCID 2733832Lithium Hexamethyldisilazide2회HCID 236461306-chloro-N-{(3S)-1-[(1S)-1-methyl-2-oxo-2-piperidin-1-ylethyl]-2-oxopyrrolidin-3-yl}naphthalene-2-sulfonamide

생성물 1

HCID 865938636-Chloro-N-(cyanomethyl)-N-{(3S)-1-[(1S)-1-methyl-2-oxo-2-piperidin-1-ylethyl]-2-oxopyrrolidin-3-yl}naphthalene-2-sulfonamide수율 43%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

반응 조건

온도
-78 °C

실험 절차

A solution of 6-chloro-N-{(3S)-1-[(1S)-1-methyl-2-oxo-2-piperidin-1-ylethyl]-2-oxopyrrolidin-3-yl}naphthalene-2-sulfonamide (0.015 g) in THF (2 ml) was cooled to −78° C. under nitrogen, and treated with lithium bis(trimethylsilyl) amide (1.0M solution in THF; 0.042 ml), followed by bromoacetonitrile (0.019 g). The resultant solution was allowed to reach room temperature and stirred for a further 16 h. The mixture was then cooled to −78° C. and further lithium bis(trimethylsilyl) amide (0.042 ml) added. After reaching room temperature, the reaction mixture was stirred for a further 18 h and then quenched by the addition of methanol (1 ml). The resultant solution was concentrated under reduced pressure and the residue partitioned between water and DCM. The organic layer was separated, dried (over magnesium sulphate) and concentrated under reduced pressure. The residue was purified by mass directed preparative h.p.l.c to give the title compound (0.007 g) as a colourless gum.

후처리

  1. customto reach room temperature
  2. customAfter reaching room temperature
  3. stirringthe reaction mixture was stirred for a further 18 h
  4. customquenched by the addition of methanol (1 ml)
  5. concentrationThe resultant solution was concentrated under reduced pressure
  6. customthe residue partitioned between water and DCM
  7. customThe organic layer was separated
  8. dry with materialdried (over magnesium sulphate)
  9. concentrationconcentrated under reduced pressure
  10. customThe residue was purified by mass

출처 및 근거

ORD 기록
ord-df5abb0d36a745ff964e2f8fa27724ba
출처 데이터셋
uspto-grants-2006_08
특허 번호
US07084139B2

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