Hydrochloric Acid → HCID 70479528, compound
Reaction equation
[CH2:1]([O:3][C@@H:4]1[C@@H:21]([OH:22])[CH2:20][C@@:19]2([CH3:23])[C@@H:6]([CH2:7][CH2:8][C@@H:9]3[C@@H:18]2[C@H:17]([NH:24][CH2:25][CH2:26][CH:27]([CH3:29])[CH3:28])[CH2:16][C@@:14]2([CH3:15])[C@H:10]3[CH2:11][CH2:12][C@@H:13]2[C:30]([O:32][CH3:33])=[O:31])[CH2:5]1)[CH3:2].O.[ClH:35]>>[ClH:35].[CH2:1]([O:3][C@@H:4]1[C@@H:21]([OH:22])[CH2:20][C@@:19]2([CH3:23])[C@@H:6]([CH2:7][CH2:8][C@@H:9]3[C@@H:18]2[C@H:17]([NH:24][CH2:25][CH2:26][CH:27]([CH3:28])[CH3:29])[CH2:16][C@@:14]2([CH3:15])[C@H:10]3[CH2:11][CH2:12][C@@H:13]2[C:30]([O:32][CH3:33])=[O:31])[CH2:5]1)[CH3:2]Participants
4
Procedure
Methyl 3α-ethoxy-2β-hydroxy-11α-(3-methylbutylamino)-5α-androstane-17β carboxylate (100 mg) was dissolved in 0.0987M HCl solution (2.2 ml) as far as possible. The mixture was made up to 15 g the addition of water and filtered. The residue was collected, dried and weighed. This gave a 0.56% solution with respect to free base, pH 2.2.
Workup
- filtrationfiltered
- customThe residue was collected
- customdried
Sources & evidence
- ORD record
- ord-59d85bf2e0c64eec99dce727a971c5f8
- Source dataset
- uspto-grants-1985_02
- Patent number
- US04497805
Reaction notes
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