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Diisopropylethylamine → (Z)-1-(3,3-difluoroazetidin-1-yl)-3-iodoprop-2-en-1-one

HRID 1500381
ノート
印刷プレビュー

反応式

HRID 1500381 の反応式
[I:1]/[CH:2]=[CH:3]\[C:4]([OH:6])=O.CCN(C(C)C)C(C)C.CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.Cl.[F:41][C:42]1([F:46])[CH2:45][NH:44][CH2:43]1>C(Cl)Cl.CCCCCC.C(OCC)(=O)C>[F:41][C:42]1([F:46])[CH2:45][N:44]([C:4](=[O:6])/[CH:3]=[CH:2]\[I:1])[CH2:43]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 81531DiisopropylethylamineHCID 643796(Z)-3-Iodoacrylic acidHCID 27582473,3-Difluoroazetidine hydrochlorideHCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)

生成物 1

HCID 86730374(Z)-1-(3,3-difluoroazetidin-1-yl)-3-iodoprop-2-en-1-one収率 52.33%

試薬・触媒・溶媒

3
HCID 6344Dichloromethane溶媒HCID 8058Hexane溶媒HCID 8857Ethyl Acetate溶媒

反応条件

温度
0 °C

実験手順

In a 25-mL, three-necked, round-bottomed flask equipped with nitrogen inlet and a rubber septum, (Z)-3-iodoacrylic acid (0.250 g, 1.0 eq.) was dissolved in DCM (10 mL, 40 V). The reaction mixture was cooled to 0° C., and DIPEA (0.168 g, 1.1 eq), HATU (0.494 g, 1.1 eq) and 3,3-difluoroazetidine hydrochloride (0.179 g, 1.1) were added. The reaction mixture was stirred at 0° C. for 2-3 hr. The progress of the reaction was followed by TLC analysis on silica gel with 40% ethyl acetate in hexane. The reaction mixture was filtered and concentrated by rotary evaporation (25° C., 20 mmHg) to afford 0.3 g of crude compound which was purified by column chromatography using silica 60/120 using 40% ethyl acetate in hexane as mobile phase. The column (5×10 cm) was packed in 5% ethyl acetate in hexane and started eluting in ethyl acetate in gradient manner starting with fraction collection (50-mL fractions) from 20% to 30% ethyl acetate in hexane. Compound started eluting with 20% ethyl acetate in hexane. Fractions containing such TLC profile were combined to obtain 0.18 g of desired compound (yield 52.33%). Mass: [M+H]+:273.8.

後処理

  1. customIn a 25-mL, three-necked, round-bottomed flask equipped with nitrogen inlet
  2. filtrationThe reaction mixture was filtered
  3. concentrationconcentrated by rotary evaporation (25° C., 20 mmHg)
  4. customto afford 0.3 g of crude compound which
  5. customwas purified by column chromatography
  6. washstarted eluting in ethyl acetate in gradient manner
  7. customstarting with fraction collection (50-mL fractions) from 20% to 30% ethyl acetate in hexane
  8. washCompound started eluting with 20% ethyl acetate in hexane
  9. additionFractions containing such TLC profile

出典と根拠

ORDレコード
ord-b05b147725584d30ad922a130dcb974d
出典データセット
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09206158B2

反応ノート

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