Potassium Cation → HCID 59144181, compound

HRID 2310644Notes

Reaction equation

HRID 2310644 reaction equation
[C:28](=[O:29])([O-:30])[O-:31].[CH3:39][CH2:40][O:41][C:42](=[O:43])[CH3:44].[I:1][CH2:2][CH2:3][S:4][c:5]1[c:6]([NH:14][CH:15]2[CH2:16][CH2:17][N:18]([C:21](=[O:22])[O:23][C:24]([CH3:25])([CH3:26])[CH3:27])[CH2:19][CH2:20]2)[cH:7][c:8]([N+:11](=[O:12])[O-:13])[cH:9][cH:10]1.[K+:32].[K+:33].[O:34]=[CH:35][N:36]([CH3:37])[CH3:38]>>[CH2:2]1[CH2:3][S:4][c:5]2[c:6]([cH:7][c:8]([N+:11](=[O:12])[O-:13])[cH:9][cH:10]2)[N:14]1[CH:15]1[CH2:16][CH2:17][N:18]([C:21](=[O:22])[O:23][C:24]([CH3:25])([CH3:26])[CH3:27])[CH2:19][CH2:20]1

Participants

6

Reactant 5

HCID 813Potassium Cation2×HCID 6228DimethylformamideHCID 8857Ethyl AcetateHCID 19660Carbonate IonHCID 59144149Tert-butyl 4-(2-(2-iodoethylthio)-5-nitrophenylamino)piperidine-1-carboxylate

Product 1

HCID 59144181HCID 59144181, compound

Sources & evidence

ORD record
ord-68b9980aa7424cc3afb4fcf2c3a94f39
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (10/10)

Reaction notes

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