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4-Chlorobenzenesulfonyl chloride → HCID 178523319, compound

HRID 309915
Notes
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Reaction equation

HRID 309915 reaction equation
[Cl:28][c:29]1[cH:30][cH:31][c:32]([S:35](=[O:36])(=[O:37])[Cl:38])[cH:33][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:35]([c:32]1[cH:31][cH:30][c:29]([Cl:28])[cH:34][cH:33]1)(=[O:36])=[O:37])[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 73984-Chlorobenzenesulfonyl chlorideHCID 333428N2-((9H-Fluoren-9-ylmethoxy)carbonyl)lysine

Product 1

HCID 178523319HCID 178523319, compound

Sources & evidence

ORD record
ord-2e7e57ab094d4797b6490296c6e6fc89
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (8/10)
DOI
10.1039/C8SC04228D

Reaction notes

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On this pageParticipantsSources & evidenceReaction notes