Hydrochloric Acid → HCID 21190243, compound
Reaction equation
C(OC([N:8]1[CH2:18][C:17]2[N:19]3[C:10](=[CH:11][N:12]=[C:13]3[CH:14]=[CH:15][CH:16]=2)[C:9]1=[O:20])=O)(C)(C)C.[ClH:21]>C(O)C>[ClH:21].[N:12]1[CH:11]=[C:10]2[N:19]3[C:17](=[CH:16][CH:15]=[CH:14][C:13]=13)[CH2:18][NH:8][C:9]2=[O:20]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 95.7 mg (0.35 mmol) of 4,5-dihydro-4-(tert-butoxycarbonyl)-3H-1,4,8b-triazaacenaphthylen-3-one in 100 ml of ethanol was added 0.09 ml (1.05 mmol) of 12N HCl. The mixture was stirred for one hour at room temperature. The resulting crystalline precipitates were collected by filtration, washed with a small volume of ethanol and ether and dried to give 56.1 mg of the desired compound (76.4%, white solid).
Workup
- customThe resulting crystalline precipitates
- filtrationwere collected by filtration
- washwashed with a small volume of ethanol and ether
- customdried
Sources & evidence
- ORD record
- ord-8b1f0ecf0d4d49329ca2b8c87d244720
- Source dataset
- uspto-grants-2001_06
- Patent number
- US06251905B1
Reaction notes
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