L-Lysine → HCID 70294375, compound

HRID 365429Notes

Reaction equation

HRID 365429 reaction equation
N[C@H:2]([C:8](O)=[O:9])CCCCN.[NH2:11][CH2:12][CH2:13][CH2:14][CH2:15][C@H:16]([NH:20][C:21]([C@H:23]([N:31]([CH3:56])[C:32]([C@H:34]([NH:46][C:47](=[O:55])/[CH:48]=[CH:49]/[CH2:50][C:51]([NH2:54])([CH3:53])[CH3:52])[CH2:35][C:36]1[CH:45]=[CH:44][C:43]2[C:38](=[CH:39][CH:40]=[CH:41][CH:42]=2)[CH:37]=1)=[O:33])[CH2:24][C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1)=[O:22])[C:17](=[O:19])[NH2:18]>>[C:8]([NH:11][CH2:12][CH2:13][CH2:14][CH2:15][C@H:16]([NH:20][C:21]([C@H:23]([N:31]([CH3:56])[C:32]([C@H:34]([NH:46][C:47](=[O:55])/[CH:48]=[CH:49]/[CH2:50][C:51]([NH2:54])([CH3:53])[CH3:52])[CH2:35][C:36]1[CH:45]=[CH:44][C:43]2[C:38](=[CH:39][CH:40]=[CH:41][CH:42]=2)[CH:37]=1)=[O:33])[CH2:24][C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1)=[O:22])[C:17](=[O:19])[NH2:18])(=[O:9])[CH3:2]

Participants

3

Reactant 2

HCID 5962L-LysineHCID 70293356HCID 70293356, compound

Product 1

HCID 70294375HCID 70294375, compound

Procedure

This compound was prepared by acetylation of the epsilon amino group in the lysine fragment using the general method described above and using the compound prepared in example 19 as starting material.

Sources & evidence

ORD record
ord-86f530402cce48e7a9768f0ab411cd61
Source dataset
uspto-grants-2000_10
Patent number
US06127341

Reaction notes

Loading…