HCID 68537906, compound → N-(5-Phenyl-1,3,4-thiadiazol-2-yl)glycine
Reaction equation
C([O:5][C:6](=[O:20])[CH2:7][NH:8][C:9]1[S:10][C:11]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)=[N:12][N:13]=1)(C)(C)C>C(O)(C(F)(F)F)=O.ClCCl>[C:14]1([C:11]2[S:10][C:9]([NH:8][CH2:7][C:6]([OH:20])=[O:5])=[N:13][N:12]=2)[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
290 mg (0.99 mmol) of (5-phenyl-[1,3,4]thiadiazol-2-ylamino)-acetic acid tert-butyl ester in 5 ml of TFA and 5 ml of dichloromethane at room temperature for 16 h. The volatiles were removed under reduced pressure.
Workup
- customThe volatiles were removed under reduced pressure
Sources & evidence
- ORD record
- ord-8ad03fd5f43a4a7496f03b8d72b07384
- Source dataset
- uspto-grants-2012_05
- Patent number
- US08188291B2
Reaction notes
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