HCID 20373034, compound → HCID 20373040, compound
Reaction equation
C(OC([NH:8][CH2:9][CH2:10][CH2:11][N:12]1[C:33](=[O:34])[N:15]2[C:16]3[CH:31]=[CH:30][C:29]([Cl:32])=[CH:28][C:17]=3[N:18]([C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=3)[C:19](=[O:21])[CH:20]=[C:14]2[NH:13]1)=O)(C)(C)C>FC(F)(F)C(O)=O>[NH2:8][CH2:9][CH2:10][CH2:11][N:12]1[C:33](=[O:34])[N:15]2[C:16]3[CH:31]=[CH:30][C:29]([Cl:32])=[CH:28][C:17]=3[N:18]([C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=3)[C:19](=[O:21])[CH:20]=[C:14]2[NH:13]1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
2.5 g of 2-[3-(t-butoxycarbonylamino)propyl]-8-chloro-6-phenyl-1H-s-triazolo[4,3-a][1,5]benzodiazepine-1,5-dione in 50 ml of trifluoroacetic acid is stirred at room temperature for 2 hours. The reaction is evaporated and the residue is stirred with a solution of 1.9 g of sodium bicarbonate in 400 ml of methanol-water (10:1). After 3 hours the reaction is evaporated and the residue is partitioned between methylene chloride and water. The methylene chloride is washed with water, dried and evaporated to give the title compound.
Workup
- customThe reaction is evaporated
- customAfter 3 hours the reaction is evaporated
- customthe residue is partitioned between methylene chloride and water
- washThe methylene chloride is washed with water
- customdried
- customevaporated
Sources & evidence
- ORD record
- ord-d316aabc4ecb475b80d3b020d55d562e
- Source dataset
- uspto-grants-1978_01
- Patent number
- US04070355
Reaction notes
Loading…