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2-Mesitylenesulfonyl chloride → HCID 178425958, compound

HRID 182794
Notes
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Reaction equation

HRID 182794 reaction equation
[CH3:28][c:29]1[c:30]([S:37](=[O:38])(=[O:39])[Cl:40])[c:31]([CH3:36])[cH:32][c:33]([CH3:35])[cH:34]1.[cH:1]1[cH:2][cH:3][cH:4][c:5]2[c:13]1[CH:12]([CH2:14][O:15][C:16](=[O:17])[NH:18][CH:19]([CH2:20][CH2:21][CH2:22][CH2:23][NH2:24])[C:25](=[O:26])[OH:27])[c:11]1[c:6]-2[cH:7][cH:8][cH:9][cH:10]1>>[cH:1]1[cH:2][cH:3][cH:4][c:5]2[c:13]1[CH:12]([CH2:14][O:15][C:16](=[O:17])[NH:18][CH:19]([CH2:20][CH2:21][CH2:22][CH2:23][NH:24][S:37]([c:30]1[c:29]([CH3:28])[cH:34][c:33]([CH3:35])[cH:32][c:31]1[CH3:36])(=[O:38])=[O:39])[C:25](=[O:26])[OH:27])[c:11]1[c:6]-2[cH:7][cH:8][cH:9][cH:10]1
ParticipantsSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 130462-Mesitylenesulfonyl chlorideHCID 333428N2-((9H-Fluoren-9-ylmethoxy)carbonyl)lysine

Product 1

HCID 178425958HCID 178425958, compound

Sources & evidence

ORD record
ord-bb0eeba334cc48b18217f74f20e9561c
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (6/10)
DOI
10.1039/C8SC04228D

Reaction notes

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On this pageParticipantsSources & evidenceReaction notes