Ammonium → HCID 22272818, compound

HRID 676168Notes

Reaction equation

HRID 676168 reaction equation
[Br:17][CH2:18][C:19](=[O:20])[NH:21][c:22]1[c:23]([CH:32]([CH3:33])[CH3:34])[cH:24][c:25]([OH:31])[cH:26][c:27]1[CH:28]([CH3:29])[CH3:30].[C:11](=[O:12])([O-:13])[O-:14].[CH3:37][C:38]#[N:39].[Cl-:35].[K+:15].[K+:16].[NH4+:36].[OH:1][CH2:2][CH2:3][CH2:4][N:5]1[CH2:6][CH2:7][NH:8][CH2:9][CH2:10]1>>[OH:1][CH2:2][CH2:3][CH2:4][N:5]1[CH2:6][CH2:7][N:8]([CH2:18][C:19](=[O:20])[NH:21][c:22]2[c:23]([CH:32]([CH3:33])[CH3:34])[cH:24][c:25]([OH:31])[cH:26][c:27]2[CH:28]([CH3:29])[CH3:30])[CH2:9][CH2:10]1

Participants

8

Reactant 7

HCID 223AmmoniumHCID 312ChlorideHCID 813Potassium Cation2×HCID 6342AcetonitrileHCID 19660Carbonate IonHCID 79207Piperazin-1-ylpropanolHCID 99666052-Bromo-N-[4-hydroxy-2,6-bis(1-methylethyl)phenyl]acetamide

Product 1

HCID 22272818HCID 22272818, compound

Sources & evidence

ORD record
ord-9505f28974b04182ad2e7aad9d6bc4b5
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (3/10)

Reaction notes

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