Carbamic acid, [3-(bromoacetyl)phenyl]-, ethyl ester → HCID 178419570, compound

HRID 236641

Reaction equation

HRID 236641 reaction equation
[Br:1][CH2:2][C:3]([C:5]1[CH:6]=[C:7]([NH:11][C:12](=[O:16])[O:13][CH2:14][CH3:15])[CH:8]=[CH:9][CH:10]=1)=O.[C:17]([NH:20][C:21]([NH2:23])=[S:22])(=[NH:19])[NH2:18]>C(O)C>[BrH:1].[NH:20]([C:21]1[S:22][CH:2]=[C:3]([C:5]2[CH:6]=[C:7]([NH:11][C:12](=[O:16])[O:13][CH2:14][CH3:15])[CH:8]=[CH:9][CH:10]=2)[N:23]=1)[C:17]([NH2:19])=[NH:18]

Participants

4

Reactant 2

HCID 20216369Carbamic acid, [3-(bromoacetyl)phenyl]-, ethyl esterHCID 178513045HCID 178513045, compound

Product 1

HCID 178419570HCID 178419570, compoundYield 94.9%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

A mixture of 17.17 gm of ethyl N-[3-(2-bromoacetyl)-phenyl]-carbamate, 7.1 gm of amidinothiourea and 45 ml of ethanol was refluxed for 4 hours and then cooled to room temperature. The precipitate formed thereby was filtered off and washed with cold ethanol, yielding 22 gm of the title compound, m.p. 240°-2° C.

Workup

  1. temperaturewas refluxed for 4 hours
  2. customThe precipitate formed
  3. filtrationthereby was filtered off
  4. washwashed with cold ethanol

Sources & evidence

ORD record
ord-6d885af43e5a42df8c8026180f6c9d4f
Source dataset
uspto-grants-1987_02
Patent number
US04645841

Linked notes

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