Pyridine → HCID 86742049, compound

HRID 231704Notes

Reaction equation

HRID 231704 reaction equation
[CH2:1]([N:3]([CH2:30][CH3:31])[C:4]([NH:6][C@H:7]1[CH2:21][C@H:20]2[C@@H:10]([CH2:11][C:12]3[C:22]4[C:15](=[CH:16][CH:17]=[CH:18][C:19]2=4)[NH:14][C:13]=3[C:23]#[C:24][C:25](O)(C)C)[N:9]([CH3:29])[CH2:8]1)=[O:5])[CH3:2].[N:32]1[CH:37]=CC=C[CH:33]=1>>[CH3:33][N:32]([CH3:37])[C:25]#[C:24][CH2:23][C:13]1[NH:14][C:15]2[C:22]3[C:12]=1[CH2:11][C@@H:10]1[C@@H:20]([C:19]=3[CH:18]=[CH:17][CH:16]=2)[CH2:21][C@H:7]([NH:6][C:4](=[O:5])[N:3]([CH2:1][CH3:2])[CH2:30][CH3:31])[CH2:8][N:9]1[CH3:29]

Participants

3

Procedure

1,1-diethyl-3-[2-(3-hydroxy-3-methyl-1-butynyl)-6-methyl-8α-ergolinyl]urea, mp starting with 132°-140° C., [α]D =+67.8° (c=0.2% in pyridine);

Workup

  1. customstarting with 132°-140° C.

Sources & evidence

ORD record
ord-1d5dc13df01241349a01f84f584e27de
Source dataset
uspto-grants-1989_07
Patent number
US04847262

Reaction notes

Loading…