2-(Diethylamino)ethanethiol → HCID 178454412, compound

HRID 253918

Reaction equation

HRID 253918 reaction equation
[C:1]([N:6]1[CH2:11][CH2:10][CH:9]([N:12]([C@H:24]2[CH2:29][CH2:28][C@H:27]([CH3:30])[CH2:26][CH2:25]2)[C:13]([NH:15][C:16]2[S:17][C:18]([S:21]C#N)=[CH:19][N:20]=2)=[O:14])[CH2:8][CH2:7]1)(=[O:5])[CH2:2][CH2:3][CH3:4].SC[C@@H]([C@@H](CS)O)O.[CH2:39]([N:41]([CH2:45][CH3:46])[CH2:42][CH2:43]S)[CH3:40]>>[C:1]([N:6]1[CH2:11][CH2:10][CH:9]([N:12]([C@H:24]2[CH2:29][CH2:28][C@H:27]([CH3:30])[CH2:26][CH2:25]2)[C:13]([NH:15][C:16]2[S:17][C:18]([S:21][CH2:40][CH2:39][N:41]([CH2:45][CH3:46])[CH2:42][CH3:43])=[CH:19][N:20]=2)=[O:14])[CH2:8][CH2:7]1)(=[O:5])[CH2:2][CH2:3][CH3:4]

Participants

4

Procedure

Prepared as described in general procedures (H) and (I) using 1-(1-butyryl-piperidin-4-yl)-1-(trans-4-methyl-cyclohexyl)-3-(5-thiocyanato-thiazol-2-yl)-urea, dithioerythritol and 2-diethylamino-ethanethiol

Workup

  1. customPrepared

Sources & evidence

ORD record
ord-25ce166c138d4429bdf0f521402c0865
Source dataset
uspto-grants-2011_01
Patent number
US07872139B2

Linked notes

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