1-Methylpiperazine → HCID 86735852, compound

HRID 866767Notes

Reaction equation

HRID 866767 reaction equation
Cl[C@H:2]1[CH2:19][C@@:18]2([CH3:20])[C@@H:5]([CH2:6][CH2:7][C@@H:8]3[C@@H:17]2[CH2:16][CH2:15][C@@:13]2([CH3:14])[C@H:9]3[CH2:10][C@H:11]([N:22]3[CH2:27][CH2:26][CH2:25][CH2:24][CH2:23]3)[C@@H:12]2[OH:21])[CH2:4][C@@H:3]1[OH:28].[CH3:29][N:30]1[CH2:35][CH2:34][NH:33][CH2:32][CH2:31]1>>[CH3:29][N:30]1[CH2:35][CH2:34][N:33]([C@H:2]2[CH2:19][C@@:18]3([CH3:20])[C@@H:5]([CH2:6][CH2:7][C@@H:8]4[C@@H:17]3[CH2:16][CH2:15][C@@:13]3([CH3:14])[C@H:9]4[CH2:10][C@H:11]([N:22]4[CH2:27][CH2:26][CH2:25][CH2:24][CH2:23]4)[C@@H:12]3[OH:21])[CH2:4][C@@H:3]2[OH:28])[CH2:32][CH2:31]1

Participants

3

Reactant 2

HCID 531671-MethylpiperazineHCID 22804191HCID 22804191, compound

Product 1

HCID 86735852HCID 86735852, compound

Procedure

The compound was prepared according to Example 5 from 2β-chloro-3α-,17β-dihydroxy-16β-piperidino-5α-androstane and from N-methyl-piperazine.

Workup

  1. customThe compound was prepared

Sources & evidence

ORD record
ord-113a0858fe6d45eeaffbcc981b18ded1
Source dataset
uspto-grants-1978_07
Patent number
US04101545

Reaction notes

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