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Triethylamine → [(E)-(6-methoxy-2,3-dihydroinden-1-ylidene)amino] methanesulfonate

HRID 1750083
Notes
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Reaction equation

HRID 1750083 reaction equation
[CH3:1][O:2][C:3]1[CH:11]=[C:10]2[C:6]([CH2:7][CH2:8]/[C:9]/2=[N:12]\[OH:13])=[CH:5][CH:4]=1.CCN(CC)CC.[CH3:21][S:22](Cl)(=[O:24])=[O:23]>C(Cl)Cl.CN(C1C=CN=CC=1)C>[CH3:21][S:22]([O:13]/[N:12]=[C:9]1\[CH2:8][CH2:7][C:6]2[C:10]\1=[CH:11][C:3]([O:2][CH3:1])=[CH:4][CH:5]=2)(=[O:24])=[O:23]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 3

HCID 8471TriethylamineHCID 31297Methanesulfonyl chlorideHCID 11389720Oxime-2,3-dihydro-6-methoxy-1H-inden-1-one

Product 1

HCID 89350921[(E)-(6-methoxy-2,3-dihydroinden-1-ylidene)amino] methanesulfonateYield 7,750%

Reagents, catalysts & solvents 2

HCID 142844-(Dimethylamino)pyridineCatalyst
HCID 6344
Dichloromethane
Solvent

Procedure

To the solution of intermediate 16 (6.6 g, 37.2 mmol) in CH2Cl2 (120 mL) was added Et3N (20.6 mL, 149 mmol), DMAP (455 mg, 3.73 mmol) and MsCl (4.35 mL, 55.87 mmol). The mixture was stirred at rt overnight. The reaction mixture was washed successively with water, saturated aq NH4Cl, brine, dried over anhydrous MgSO4, filtered and concentrated. The crude product was purified by flash chromatography on silica gel column (elution with PE/CH2Cl2=1:1) to give (E)-6-methoxy-2,3-dihydro-1H-inden-1-one O-methylsulfonyl oxime (intermediate 17) (736 g, 82%) as a white solid.

Workup

  1. washThe reaction mixture was washed successively with water, saturated aq NH4Cl, brine
  2. dry with materialdried over anhydrous MgSO4
  3. filtrationfiltered
  4. concentrationconcentrated
  5. customThe crude product was purified by flash chromatography on silica gel column (elution with PE/CH2Cl2=1:1)

Sources & evidence

ORD record
ord-fccb115ae67b4acbbabfe096266fff67
Source dataset
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09156822B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes