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Ammonium → HCID 57503228, compound

HRID 1545490
Notes
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Reaction equation

HRID 1545490 reaction equation
[CH3:35][CH2:36][OH:37].[CH:1](=[O:2])[CH:3]1[CH2:4][N:5]=[C:6]([c:8]2[nH:9][c:10]3[c:11]([N:17]([S:18](=[O:19])(=[O:20])[c:21]4[n:22][cH:23][cH:24][cH:25][cH:26]4)[CH3:27])[cH:12][cH:13][cH:14][c:15]3[cH:16]2)[S:7]1.[Cl-:28].[NH4+:29].[O:30]1[CH2:31][CH2:32][CH2:33][CH2:34]1>>[CH2:1]([OH:2])[CH:3]1[CH2:4][N:5]=[C:6]([c:8]2[nH:9][c:10]3[c:11]([N:17]([S:18](=[O:19])(=[O:20])[c:21]4[n:22][cH:23][cH:24][cH:25][cH:26]4)[CH3:27])[cH:12][cH:13][cH:14][c:15]3[cH:16]2)[S:7]1
ParticipantsSources & evidenceReaction notes

Participants

6

Reactant 5

HCID 223AmmoniumHCID 312ChlorideHCID 702EthanolHCID 8028TetrahydrofuranHCID 57503229N-[2-(5-formyl-4,5-dihydro-1,3-thiazol-2-yl)-1H-indol-7-yl]-N-methylpyridine-2-sulfonamide

Product 1

HCID 57503228HCID 57503228, compound

Sources & evidence

ORD record
ord-219bf0c2746a4d27871cbdf2a8815ef8
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (1/10)
DOI
10.1039/C8SC04228D

Reaction notes

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On this pageParticipantsSources & evidenceReaction notes