Chloride → HCID 178473345, compound

HRID 1112999Notes

Reaction equation

HRID 1112999 reaction equation
[C:32]([BH3-:33])#[N:34].[CH3:17][O-:18].[CH3:36][OH:37].[Cl-:38].[Cl-:40].[NH:1]1[CH2:2][CH2:3][CH:4]([N:7]2[C:8](=[O:16])[CH2:9][CH:10]3[CH2:11][CH2:12][CH2:13][CH2:14][CH:15]23)[CH2:5][CH2:6]1.[Na+:19].[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]>>[N:1]1([CH:21]2[CH2:22][CH2:23][N:24]([C:27](=[O:28])[O:29][CH2:30][CH3:31])[CH2:25][CH2:26]2)[CH2:2][CH2:3][CH:4]([N:7]2[C:8](=[O:16])[CH2:9][CH:10]3[CH2:11][CH2:12][CH2:13][CH2:14][CH:15]23)[CH2:5][CH2:6]1

Participants

9

Reactant 8

HCID 312Chloride2×HCID 887MethanolHCID 923Sodium ion2×HCID 32051Zinc(2+)HCID 34767Ethyl 4-oxo-1-piperidinecarboxylateHCID 498716Cyano-borohydrideHCID 3826051MethoxideHCID 590254601-piperidin-4-yl-3a,4,5,6,7,7a-hexahydro-3H-indol-2-one

Product 1

HCID 178473345HCID 178473345, compound

Sources & evidence

ORD record
ord-cd96d0cd0a1b4cf288e9188f975b0184
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (7/10)

Reaction notes

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