Lawesson's reagent → HCID 136062684, compound

HRID 620174Notes

Reaction equation

HRID 620174 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[C:9]2[CH:18]=[C:17]([CH2:19][CH2:20][C:21]3[CH:26]=[CH:25][C:24]([O:27][CH3:28])=[CH:23][CH:22]=3)[S:16][C:10]=2[NH:11][C:12](=O)[CH2:13][N:14]=1.COC1C=CC(P2(SP(C3C=CC(OC)=CC=3)(=S)S2)=[S:38])=CC=1>C1(C)C=CC=CC=1>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[C:9]2[CH:18]=[C:17]([CH2:19][CH2:20][C:21]3[CH:26]=[CH:25][C:24]([O:27][CH3:28])=[CH:23][CH:22]=3)[S:16][C:10]=2[NH:11][C:12](=[S:38])[CH2:13][N:14]=1

Participants

4

Reactant 2

HCID 87949Lawesson's reagentHCID 136018062HCID 136018062, compound

Product 1

HCID 136062684HCID 136062684, compoundYield 132.6%

Reagents, catalysts & solvents 1

HCID 1140TolueneSolvent

Procedure

A suspension of 7 g of 5-(2-chlorophenyl)-7-[2-(4-methoxyphenyl)ethyl]-1,3-dihydro-2H-thieno[2,3-e]-1,4-diazepin-2-one, melting at 196°-198° C. and 5 g of Lawesson reagent in 100 ml of toluene is stirred at 45°-48° C. for an hour. The resultant solution is concentrated under reduced pressure, and the residue is subjected to chromatography on silica gel and then eluted with chloroform-methanol (100:1 to 100:2). The objective fraction is concentrated under reduced pressure to give 7 g of 5-(2-chlorophenyl)-7-[2-(4-methoxyphenyl)ethyl]-1,3-dihydro-2H-thieno[2,3-e]-1,4-diazepine-2-thione, melting at 185°-186° C. with decomposition.

Workup

  1. concentrationThe resultant solution is concentrated under reduced pressure
  2. washeluted with chloroform-methanol (100:1 to 100:2)
  3. concentrationThe objective fraction is concentrated under reduced pressure

Sources & evidence

ORD record
ord-71e91387a07f4a36afccd1322d7ce9ce
Source dataset
uspto-grants-1989_04
Patent number
US04820703

Reaction notes

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