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2-(Azetidin-1-ylcarbonyl)-5-bromopyridine → HCID 178462593, compound

HRID 94057
Notes
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Reaction equation

HRID 94057 reaction equation
[CH2:1]([CH3:2])[n:3]1[n:4][c:5]([NH:8][C:9]([c:10]2[cH:11][c:12]([OH:22])[cH:13][c:14]([O:16][CH:17]([CH2:18][O:19][CH3:20])[CH3:21])[cH:15]2)=[O:23])[cH:6][cH:7]1.[N:24]1([C:28](=[O:29])[c:30]2[n:31][cH:32][c:33]([Br:36])[cH:34][cH:35]2)[CH2:25][CH2:26][CH2:27]1>>[CH2:1]([CH3:2])[n:3]1[n:4][c:5]([NH:8][C:9]([c:10]2[cH:11][c:12]([O:22][c:33]3[cH:32][n:31][c:30]([C:28]([N:24]4[CH2:25][CH2:26][CH2:27]4)=[O:29])[cH:35][cH:34]3)[cH:13][c:14]([O:16][CH:17]([CH2:18][O:19][CH3:20])[CH3:21])[cH:15]2)=[O:23])[cH:6][cH:7]1
ParticipantsSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 536296172-(Azetidin-1-ylcarbonyl)-5-bromopyridineHCID 72524174N-(1-ethylpyrazol-3-yl)-3-hydroxy-5-(1-methoxypropan-2-yloxy)benzamide

Product 1

HCID 178462593HCID 178462593, compound

Sources & evidence

ORD record
ord-29d22349e46441ffa8a3a3eebc42d66a
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (2/10)
DOI
10.1039/C8SC04228D

Reaction notes

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On this pageParticipantsSources & evidenceReaction notes