1,4-Dioxa-8-azaspiro(4.5)decane → HCID 67684001, compound
Reaction equation
[O:1]1[C@H:3]2[CH2:4][C@H:5]3[C@:18]([CH3:20])([CH2:19][C@@H:2]12)[C@@H:17]1[C@H:8]([C@H:9]2[C@@:13]([CH2:15][CH2:16]1)([CH3:14])[C@@H:12]([OH:21])[C@@H:11]([N:22]1[CH2:27][CH2:26][CH2:25][CH2:24][CH2:23]1)[CH2:10]2)[CH2:7][CH2:6]3.[O:28]1[C:32]2([CH2:37][CH2:36][NH:35][CH2:34][CH2:33]2)[O:31][CH2:30][CH2:29]1>>[O:28]1[C:32]2([CH2:37][CH2:36][N:35]([C@H:2]3[CH2:19][C@@:18]4([CH3:20])[C@@H:5]([CH2:6][CH2:7][C@@H:8]5[C@@H:17]4[CH2:16][CH2:15][C@@:13]4([CH3:14])[C@H:9]5[CH2:10][C@H:11]([N:22]5[CH2:23][CH2:24][CH2:25][CH2:26][CH2:27]5)[C@@H:12]4[OH:21])[CH2:4][C@@H:3]3[OH:1])[CH2:34][CH2:33]2)[O:31][CH2:30][CH2:29]1Participants
3
Procedure
2α,3α-Epoxy-16β-(1-piperidinyl)-5α-androstane-17β-ol is reacted with 1,4-dioxa-8-azaspiro[4.5]decane as described in Example 3 to give the title compound in a yield of 79.88%, m.p.: 216°-218° C.
Sources & evidence
- ORD record
- ord-2eab8f05c2064e67bee4fe11922bce09
- Source dataset
- uspto-grants-1997_01
- Patent number
- US05591735
Reaction notes
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