Diisopropylamine → HCID 13772093, compound

HRID 142292

Reaction equation

HRID 142292 reaction equation
[CH2:39]1[O:40][CH2:41][CH2:42][CH2:43]1.[CH3:8][CH:9]([CH3:10])[N:11]([CH2:12][CH2:13][CH:14]([C:15](=[O:16])[O:17][CH3:18])[c:19]1[c:20]([Cl:25])[cH:21][cH:22][cH:23][cH:24]1)[CH:26]([CH3:27])[CH3:28].[CH:1]([NH:2][CH:3]([CH3:4])[CH3:5])([CH3:6])[CH3:7].[Cl:29][CH2:30][C:31](=[O:32])[N:33]1[CH2:34][CH2:35][CH2:36][CH2:37][CH2:38]1>>[CH3:8][CH:9]([CH3:10])[N:11]([CH2:12][CH2:13][C:14]([C:15](=[O:16])[O:17][CH3:18])([c:19]1[c:20]([Cl:25])[cH:21][cH:22][cH:23][cH:24]1)[CH2:30][C:31](=[O:32])[N:33]1[CH2:34][CH2:35][CH2:36][CH2:37][CH2:38]1)[CH:26]([CH3:27])[CH3:28]

Participants

5

Reactant 4

HCID 7912DiisopropylamineHCID 8028TetrahydrofuranHCID 2223122-Chloro-1-piperidine-1-yl-ethanoneHCID 13772096HCID 13772096, compound

Product 1

HCID 13772093HCID 13772093, compound

Sources & evidence

ORD record
ord-88fbc9e7010644a0b8ca9db513b8ee07
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (9/10)

Linked notes

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