Ammonium → HCID 18679742, compound

HRID 206427

Reaction equation

HRID 206427 reaction equation
[Br-:13].[CH2:14]([Mg+:15])[CH3:16].[CH3:17][O:18][c:19]1[c:20]([N+:30](=[O:31])[O-:32])[c:21]2[c:26]([cH:27][cH:28]1)[C:25](=[O:29])[CH2:24][CH2:23][CH2:22]2.[Cl-:33].[Cl:35][CH2:36][Cl:37].[I:1][c:2]1[n:3][cH:4][n:5]([S:7](=[O:8])(=[O:9])[N:10]([CH3:11])[CH3:12])[cH:6]1.[NH4+:34]>>[c:2]1([C:25]2([OH:29])[CH2:24][CH2:23][CH2:22][c:21]3[c:20]([N+:30](=[O:31])[O-:32])[c:19]([O:18][CH3:17])[cH:28][cH:27][c:26]32)[n:3][cH:4][n:5]([S:7](=[O:8])(=[O:9])[N:10]([CH3:11])[CH3:12])[cH:6]1

Participants

8

Reactant 7

HCID 223AmmoniumHCID 259Bromide ionHCID 312ChlorideHCID 6344DichloromethaneHCID 2773390N,N-Dimethyl 4-iodo-1H-imidazole-1-sulfonamideHCID 130673376-Methoxy-5-nitro-1,2,3,4-tetrahydronaphthalen-1-oneHCID 178461628HCID 178461628, compound

Product 1

HCID 18679742HCID 18679742, compound

Sources & evidence

ORD record
ord-658e156452eb4c788718a40a8f2281b9
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (6/10)

Linked notes

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