Trifluoroacetic acid → HCID 57670971, compound

HRID 1364333Notes

Reaction equation

HRID 1364333 reaction equation
COC[O:4][C:5]1[CH:30]=[CH:29][C:28]([CH3:31])=[CH:27][C:6]=1/[CH:7]=[C:8]1/[C:9](=[O:26])[N:10]([S:16]([C:19]2[CH:24]=[CH:23][C:22]([Cl:25])=[CH:21][CH:20]=2)(=[O:18])=[O:17])[CH2:11][C:12](=[O:15])[NH:13][CH2:14]/1.FC(F)(F)C(O)=O>C(Cl)Cl>[OH:4][C:5]1[CH:30]=[CH:29][C:28]([CH3:31])=[CH:27][C:6]=1/[CH:7]=[C:8]1/[C:9](=[O:26])[N:10]([S:16]([C:19]2[CH:20]=[CH:21][C:22]([Cl:25])=[CH:23][CH:24]=2)(=[O:17])=[O:18])[CH2:11][C:12](=[O:15])[NH:13][CH2:14]/1

Participants

4

Reactant 2

HCID 6422Trifluoroacetic acidHCID 66935148HCID 66935148, compound

Product 1

HCID 57670971HCID 57670971, compoundYield 101.2%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

To (6E)-6-[2-(methoxymethoxy)-5-methylbenzylidene]-4-[(4-chlorophenyl)sulfonyl]-1,4-diazepan-2,5-dione (95 mg), synthesized by using, instead of the starting material of Reference Example 117, that is, the compound S6, the compound S11 for the similar procedure as in Reference Example 117, Reference Example 122, and Example 1, in methylene chloride (0.48 ml) solution, trifluoroacetic acid (0.48 ml) was added and the mixture was stirred at room temperature for 45 minutes. Next, the reaction solution was concentrated, and the residue was recrystallized from hexane/ethyl acetate to obtain the title compound (87 mg).

Workup

  1. concentrationNext, the reaction solution was concentrated
  2. customthe residue was recrystallized from hexane/ethyl acetate

Sources & evidence

ORD record
ord-e33d6f7c91854f5fab384bdbb7ed96e5
Source dataset
uspto-grants-2011_02
Patent number
US07888348B2

Reaction notes

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