Ethyl Acetate → HCID 68538138, compound

Reaction equation

[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6](=[O:7])[N:8]1[CH2:9][CH2:10][CH:11]([O:14][c:15]2[n:16][cH:17][cH:18][c:19]([N+:21]([O-:22])=[O:23])[cH:20]2)[CH2:12][CH2:13]1.[CH3:26][CH2:27][O:28][C:29]([CH3:30])=[O:31].[H:24][H:25]>>[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6](=[O:7])[N:8]1[CH2:9][CH2:10][CH:11]([O:14][c:15]2[n:16][cH:17][cH:18][c:19]([NH2:21])[cH:20]2)[CH2:12][CH2:13]1

Participants

Reactant 3

HCID 8857Ethyl Acetate

HCID 685380211,1-Dimethylethyl 4-[(4-nitro-2-pyridinyl)oxy]-1-piperidinecarboxylate

HCID 178418361HCID 178418361, compound

Product 1

HCID 68538138HCID 68538138, compound

Sources & evidence

ORD record: ord-00e316ff51184a3699752eb34117f462
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (7/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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