Dithioerythritol → HCID 178461385, compound

HRID 253910Notes

Reaction equation

HRID 253910 reaction equation
[CH:1]1([N:7]([C@H:19]2[CH2:24][CH2:23][C@H:22]([CH3:25])[CH2:21][CH2:20]2)[C:8]([NH:10][C:11]2[S:12][C:13]([S:16]C#N)=[CH:14][N:15]=2)=[O:9])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.SC[C@@H]([C@@H](CS)O)O.[N:34](=[CH:42][CH2:43]Cl)[CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40]Cl>>[N:34]1([CH2:42][CH2:43][S:16][C:13]2[S:12][C:11]([NH:10][C:8](=[O:9])[N:7]([CH:1]3[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]3)[C@H:19]3[CH2:20][CH2:21][C@H:22]([CH3:25])[CH2:23][CH2:24]3)=[N:15][CH:14]=2)[CH2:40][CH2:39][CH2:38][CH2:37][CH2:36][CH2:35]1

Participants

4

Reactant 3

HCID 439352DithioerythritolHCID 534452782-(Hexamethyleneimino)ethyl chlorideHCID 178461390HCID 178461390, compound

Product 1

HCID 178461385HCID 178461385, compound

Procedure

Prepared as described in general procedure (H) using 1-cyclohexyl-1-(trans-4-methyl-cyclohexyl)-3-(5-thiocyanato-thiazol-2-yl)-urea, dithioerythritol and 2-(hexamethyleneimino)ethyl chloride.

Workup

  1. customPrepared

Sources & evidence

ORD record
ord-8127f79931d04aa6ae06d20ba7a652c3
Source dataset
uspto-grants-2011_01
Patent number
US07872139B2

Reaction notes

Loading…