Potassium Cation → HCID 59144148, compound

HRID 169981Notes

Reaction equation

HRID 169981 reaction equation
[C:25](=[O:26])([O-:27])[O-:28].[CH3:40][CH2:41][O:42][C:43](=[O:44])[CH3:45].[Cl:1][c:2]1[c:3]([NH:11][CH:12]2[CH2:13][CH2:14][N:15]([C:18](=[O:19])[O:20][C:21]([CH3:22])([CH3:23])[CH3:24])[CH2:16][CH2:17]2)[cH:4][c:5]([N+:8](=[O:9])[O-:10])[cH:6][cH:7]1.[K+:29].[K+:30].[O:35]=[CH:36][N:37]([CH3:38])[CH3:39].[SH:31][CH2:32][CH2:33][OH:34]>>[c:2]1([S:31][CH2:32][CH2:33][OH:34])[c:3]([NH:11][CH:12]2[CH2:13][CH2:14][N:15]([C:18](=[O:19])[O:20][C:21]([CH3:22])([CH3:23])[CH3:24])[CH2:16][CH2:17]2)[cH:4][c:5]([N+:8](=[O:9])[O-:10])[cH:6][cH:7]1

Participants

7

Reactant 6

HCID 813Potassium Cation2×HCID 15672-MercaptoethanolHCID 6228DimethylformamideHCID 8857Ethyl AcetateHCID 19660Carbonate IonHCID 59144150tert-Butyl 4-(2-chloro-5-nitrophenylamino)piperidine-1-carboxylate

Product 1

HCID 59144148HCID 59144148, compound

Sources & evidence

ORD record
ord-6b726777deb24f7882df69290a71a5cc
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (9/10)

Reaction notes

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