Ammonia → HCID 53955701, compound
Reaction equation
C([S:9][CH2:10][CH2:11][C:12]([N:14]1[C@@H:21]([C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[CH2:20][CH2:19][C@H:15]1[C:16]([OH:18])=[O:17])=[O:13])(=O)C1C=CC=CC=1.CO.N>O>[SH:9][CH2:10][CH2:11][C:12]([N:14]1[C@@H:21]([C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[CH2:20][CH2:19][C@H:15]1[C:16]([OH:18])=[O:17])=[O:13]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 25 °C
Procedure
This product from Example 3 was added to a solution of methanol saturated with ammonia and was stirred at 25° C. for 2 hours. The solvent was evaporated off, leaving a solid which was stirred in water and filtered. The filtrate was extracted five times with diethyl ether and was acidified. The acidified solution was then extracted with methylene chloride, washed with brine, dried over magnesium sulfate and concentrated to a solid. This residue was extracted with hot hexane from which the title compound crystallized, m.p. 61°-64° C.
Workup
- customThe solvent was evaporated off
- customleaving a solid which
- filtrationfiltered
- extractionThe filtrate was extracted five times with diethyl ether
- extractionThe acidified solution was then extracted with methylene chloride
- washwashed with brine
- dry with materialdried over magnesium sulfate
- concentrationconcentrated to a solid
- extractionThis residue was extracted with hot hexane from which the title compound
- customcrystallized
Sources & evidence
- ORD record
- ord-e136ca3737164aed83753717f8cc85c8
- Source dataset
- uspto-grants-1982_03
- Patent number
- US04320057
Reaction notes
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