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Pyridine → HCID 21352736, compound

HRID 2340070
Notes
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Reaction equation

HRID 2340070 reaction equation
[CH2:43]([Cl:44])[Cl:45].[CH3:1][O:2][c:3]1[cH:4][cH:5][c:6]([C:7](=[O:8])[NH:9][c:10]2[c:11]([NH:16][C:17](=[O:18])[CH:19]3[CH2:20][CH2:21][NH:22][CH2:23][CH2:24]3)[cH:12][cH:13][cH:14][cH:15]2)[cH:25][cH:26]1.[c:33]1([S:39](=[O:40])(=[O:41])[Cl:42])[cH:34][cH:35][cH:36][cH:37][cH:38]1.[cH:27]1[cH:28][cH:29][n:30][cH:31][cH:32]1>>[CH3:1][O:2][c:3]1[cH:4][cH:5][c:6]([C:7](=[O:8])[NH:9][c:10]2[c:11]([NH:16][C:17](=[O:18])[CH:19]3[CH2:20][CH2:21][N:22]([S:39]([c:33]4[cH:34][cH:35][cH:36][cH:37][cH:38]4)(=[O:40])=[O:41])[CH2:23][CH2:24]3)[cH:12][cH:13][cH:14][cH:15]2)[cH:25][cH:26]1
ParticipantsSources & evidenceReaction notes

Participants

5

Reactant 4

HCID 1049PyridineHCID 6344DichloromethaneHCID 7369Benzenesulfonyl chlorideHCID 53635745HCID 53635745, compound

Product 1

HCID 21352736HCID 21352736, compound

Sources & evidence

ORD record
ord-13db28337071432f9b716144b2d43994
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (10/10)
DOI
10.1039/C8SC04228D

Reaction notes

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On this pageParticipantsSources & evidenceReaction notes