Chloride → HCID 178456593, compound

HRID 2143294Notes

Reaction equation

HRID 2143294 reaction equation
[C:32]([BH3-:33])#[N:34].[CH2:1]([CH:2]=[CH2:3])[N:4]1[C:5](=[O:19])[N:6]([CH:13]2[CH2:14][CH2:15][NH:16][CH2:17][CH2:18]2)[CH:7]2[CH:8]1[CH2:9][CH2:10][CH2:11][CH2:12]2.[CH3:36][OH:37].[Cl-:38].[Cl-:40].[Na+:35].[O:20]=[C:21]1[CH2:22][CH2:23][N:24]([C:27](=[O:28])[O:29][CH2:30][CH3:31])[CH2:25][CH2:26]1.[Zn+2:39]>>[CH2:1]([CH:2]=[CH2:3])[N:4]1[C:5](=[O:19])[N:6]([CH:13]2[CH2:14][CH2:15][N:16]([CH:21]3[CH2:22][CH2:23][N:24]([C:27](=[O:28])[O:29][CH2:30][CH3:31])[CH2:25][CH2:26]3)[CH2:17][CH2:18]2)[CH:7]2[CH:8]1[CH2:9][CH2:10][CH2:11][CH2:12]2

Participants

8

Reactant 7

HCID 312Chloride2×HCID 887MethanolHCID 923Sodium ionHCID 32051Zinc(2+)HCID 34767Ethyl 4-oxo-1-piperidinecarboxylateHCID 498716Cyano-borohydrideHCID 178456594HCID 178456594, compound

Product 1

HCID 178456593HCID 178456593, compound

Sources & evidence

ORD record
ord-79fc7e55daae4488bd01a026fad899d5
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (4/10)

Reaction notes

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