Chloride → HCID 178452444, compound

HRID 199773Notes

Reaction equation

HRID 199773 reaction equation
[CH3:30][O:31][c:32]1[n:33][c:34]([O:35][CH3:36])[n:37][c:38]([N+:39]2([CH3:40])[CH2:41][CH2:42][O:43][CH2:44][CH2:45]2)[n:46]1.[CH3:47][OH:48].[Cl-:29].[NH2:9][c:10]1[cH:11][cH:12][c:13]([CH:16]2[O:17][CH2:18][CH2:19][N:20]([C:22](=[O:23])[O:24][C:25]([CH3:26])([CH3:27])[CH3:28])[CH2:21]2)[cH:14][cH:15]1.[nH:1]1[n:2][c:3]([C:6](=[O:7])[OH:8])[cH:4][cH:5]1>>[nH:1]1[n:2][c:3]([C:6](=[O:8])[NH:9][c:10]2[cH:11][cH:12][c:13]([CH:16]3[O:17][CH2:18][CH2:19][N:20]([C:22](=[O:23])[O:24][C:25]([CH3:26])([CH3:27])[CH3:28])[CH2:21]3)[cH:14][cH:15]2)[cH:4][cH:5]1

Participants

6

Reactant 5

HCID 312ChlorideHCID 887MethanolHCID 27340604-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholin-4-iumHCID 58315596tert-Butyl 2-(4-aminophenyl)morpholine-4-carboxylateHCID 178524567HCID 178524567, compound

Product 1

HCID 178452444HCID 178452444, compound

Sources & evidence

ORD record
ord-1b9eeb0566d64d5fb66b0756c6ab4f6f
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (6/10)

Reaction notes

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