Piperidine → HCID 22826496, compound
Reaction equation
C([O:4][C@H:5]1[CH:10]([N:11]2[CH2:16][CH2:15][CH2:14][CH2:13][CH2:12]2)[CH2:9][C@H:8]2[C@H:17]3[C@H:27]([CH2:28][CH2:29][C@:6]12[CH3:7])[C@:25]1([CH3:26])[C@H:20]([CH2:21][C@@H:22]([CH3:31])[C:23](=O)[CH2:24]1)[CH2:19][CH2:18]3)(=O)C.[NH:32]1[CH2:37][CH2:36][CH2:35][CH2:34][CH2:33]1>C(O)=O>[CH3:31][C@H:22]1[C@@H:23]([N:32]2[CH2:37][CH2:36][CH2:35][CH2:34][CH2:33]2)[CH2:24][C@@:25]2([CH3:26])[C@@H:20]([CH2:19][CH2:18][C@@H:17]3[C@@H:27]2[CH2:28][CH2:29][C@@:6]2([CH3:7])[C@H:8]3[CH2:9][C@H:10]([N:11]3[CH2:16][CH2:15][CH2:14][CH2:13][CH2:12]3)[C@@H:5]2[OH:4])[CH2:21]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
17β-Acetyloxy-3β-methyl-16-(1-piperidinyl)-5α-androstan-2-one was treated with piperidine and formic acid, as described in Example I(h), to give 3β-methyl-2β,16β-di-(1-piperidinyl)-5α-androstan-17β-ol.
Sources & evidence
- ORD record
- ord-526169d9793c410992a96e9b0c01f80d
- Source dataset
- uspto-grants-1984_05
- Patent number
- US04447425
Reaction notes
Loading…