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Pyridine → HCID 21875928, compound

HRID 673788
Notes
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Reaction equation

HRID 673788 reaction equation
[C:1]([CH2:2][CH3:3])(=[O:4])[O:5][CH2:6][CH2:7][c:8]1[cH:9][cH:10][c:11](-[n:14]2[c:15]([CH2:25][CH3:26])[n:16][c:17]3[c:18]2[n:19][cH:20][c:21]([NH2:24])[c:22]3[CH3:23])[cH:12][cH:13]1.[CH3:33][S:34]([Cl:35])(=[O:36])=[O:37].[Cl:38][CH2:39][Cl:40].[cH:27]1[cH:28][cH:29][n:30][cH:31][cH:32]1>>[C:1]([CH2:2][CH3:3])(=[O:4])[O:5][CH2:6][CH2:7][c:8]1[cH:9][cH:10][c:11](-[n:14]2[c:15]([CH2:25][CH3:26])[n:16][c:17]3[c:18]2[n:19][cH:20][c:21]([NH:24][S:34]([CH3:33])(=[O:36])=[O:37])[c:22]3[CH3:23])[cH:12][cH:13]1
ParticipantsSources & evidenceReaction notes

Participants

5

Reactant 4

HCID 1049PyridineHCID 6344DichloromethaneHCID 31297Methanesulfonyl chlorideHCID 21875554HCID 21875554, compound

Product 1

HCID 21875928HCID 21875928, compound

Sources & evidence

ORD record
ord-a6b656d4429f4a7caec533a34a917efe
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (3/10)
DOI
10.1039/C8SC04228D
On this pageParticipantsSources & evidenceReaction notes

Reaction notes

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