Water → (2S)-2-(carbamoylamino)-4-(methylsulfanyl)butanoic acid
Reaction equation
COC1C=C(CNCCCNCCC[CH2:18][NH:19][CH2:20][CH2:21][CH2:22]N)C=CC=1O.[CH3:25][S:26]CCN1CC(=O)NC1=O.ClC(Cl)(Cl)[C:38]([OH:40])=[O:39].C[N:44](C)C1C=CC(C=O)=CC=1.[OH2:54]>[NH4+].[Cl-].[NH4+].[OH-].Cl>[C:18]([NH:19][C@H:20]([C:38]([OH:40])=[O:39])[CH2:21][CH2:22][S:26][CH3:25])(=[O:54])[NH2:44]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
Mixtures of (1) 2.0 ml. of an aqueous substrate solution prepared by dissolving DL-5-(2-methylthioethyl)hydantoin in a 0.1 M NH4Cl-NH4OH buffer solution of pH 9.5 (substrate concentration: 2.0%) and (2) 2.0 ml. of the above cell suspension were prepared and placed in test tubes, respectively. The hydrolysis reaction was then carried out at 30° C. for one hour without shaking. Immediately after the completion of the reaction, 1.0 ml. of a 10% aqueous solution of trichloroacetic acid, 1.0 ml. of a 10% solution of p-dimethylaminobenzaldehyde in 6 N hydrochloric acid and 6.0 ml. of distilled water were added to each reaction mixture. Each resulting color-developed reaction mixture was centrifuged to remove insoluble materials, and the amounts of N-carbamoylmethionine produced in the reaction mixtures were colorimetrically determined by measuring the absorbance at 420 nm. As a Control, the above procedures were repeated except that no hydantoin compound was employed.
Workup
- customof an aqueous substrate solution prepared
- customof the above cell suspension were prepared
- customThe hydrolysis reaction
- customImmediately after the completion of the reaction, 1.0 ml
- customto remove insoluble materials
Sources & evidence
- ORD record
- ord-f119e163177a459f8efb89da3615bcce
- Source dataset
- uspto-grants-1980_12
- Patent number
- US04237227
Reaction notes
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