Sulfuryl chloride → HCID 54121276, compound

HRID 341747Notes

Reaction equation

HRID 341747 reaction equation
[C:1]1([N:7]2[C:11](=[O:12])[CH2:10][S:9][CH2:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.S(Cl)([Cl:16])(=O)=O>ClCCl>[Cl:16][CH:10]1[S:9][CH2:8][N:7]([C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)[C:11]1=[O:12]

Participants

4

Reactant 2

HCID 24648Sulfuryl chlorideHCID 13853396HCID 13853396, compound

Product 1

HCID 54121276HCID 54121276, compound

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

This compound was prepared by a procedure similar to that described in Preparative Example 2, Step 2 above, but using 3-phenyl-4-thiazolidinone (prepared as in Step 1 above) (0.38 g), sulphuryl chloride (0.29 g), and dichloromethane (5 ml). This product was used directly in Step 3.

Workup

  1. customThis compound was prepared by a procedure similar to

Sources & evidence

ORD record
ord-b0ce021f15c64782ac4d039a266b71a9
Source dataset
uspto-grants-1999_01
Patent number
US05856273

Reaction notes

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