4-Aminopyridine → 1H-Indole-3-acetamide, 1-[(4-fluorophenyl)methyl]-N-4-pyridinyl-

HRID 2150767Notes

Reaction equation

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

Participants

Reactant 4

HCID 17274-Aminopyridine

HCID 8028Tetrahydrofuran

HCID 10868Dicyclohexylcarbodiimide

HCID 27744362-[1-(4-fluorobenzyl)-1H-indol-3-yl]acetic acid

Product 1

HCID 98851851H-Indole-3-acetamide, 1-[(4-fluorophenyl)methyl]-N-4-pyridinyl-

Sources & evidence

ORD record: ord-4aa66efb218c42b3b47b06cc36f34838
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (4/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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