N-Acetyl-L-Cysteine → HCID 86754008, compound

HRID 1420122Notes

Reaction equation

HRID 1420122 reaction equation
[C:1]([NH:4][C@H:5]([C:8]([OH:10])=[O:9])[CH2:6][SH:7])(=[O:3])[CH3:2].[C:11]([NH:17][C@H:18]([C:21]([OH:23])=[O:22])[CH2:19][SH:20])(=[O:16])[C:12]([CH3:15])([CH3:14])[CH3:13]>>[C:1]([NH:4][C@@H:5]([CH2:6][S:7][S:20][CH2:19][C@H:18]([NH:17][C:11](=[O:16])[C:12]([CH3:14])([CH3:13])[CH3:15])[C:21]([OH:23])=[O:22])[C:8]([OH:10])=[O:9])(=[O:3])[CH3:2]

Participants

3

Reactant 2

HCID 12035N-Acetyl-L-CysteineHCID 14455343N-(2,2-Dimethyl-1-oxopropyl)-L-cysteine

Product 1

HCID 86754008HCID 86754008, compound

Procedure

The compound was obtained following the procedure given in Example 18, starting from N-acetyl-L-cysteine and N-pivaloyl-L-cysteine.

Workup

  1. customThe compound was obtained

Sources & evidence

ORD record
ord-c6e4b73eff0c4b7fb36749d0c395e65d
Source dataset
uspto-grants-1999_03
Patent number
US05889050

Reaction notes

Loading…