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2-Aminothiazole → 3-cyclopentyl-2-(1-oxo-1H-phthalazin-2-yl)-N-thiazol-2-yl-propionamide

HRID 1128251
Notes
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Reaction equation

HRID 1128251 reaction equation
[CH2:37]([Cl:38])[Cl:39].[CH:1]1([CH2:6][CH:7]([C:8](=[O:9])[OH:10])[n:11]2[c:12](=[O:21])[c:13]3[cH:14][cH:15][cH:16][cH:17][c:18]3[cH:19][n:20]2)[CH2:2][CH2:3][CH2:4][CH2:5]1.[CH:22]([N:23]([CH2:24][CH3:25])[CH:26]([CH3:27])[CH3:28])([CH3:29])[CH3:30].[s:31]1[c:32]([NH2:36])[n:33][cH:34][cH:35]1>>[CH:1]1([CH2:6][CH:7]([C:8](=[O:10])[NH:36][c:32]2[s:31][cH:35][cH:34][n:33]2)[n:11]2[c:12](=[O:21])[c:13]3[cH:14][cH:15][cH:16][cH:17][c:18]3[cH:19][n:20]2)[CH2:2][CH2:3][CH2:4][CH2:5]1
ParticipantsSources & evidenceReaction notes

Participants

5

Reactant 4

HCID 21552-AminothiazoleHCID 6344DichloromethaneHCID 81531DiisopropylethylamineHCID 66891968HCID 66891968, compound

Product 1

HCID 579191973-cyclopentyl-2-(1-oxo-1H-phthalazin-2-yl)-N-thiazol-2-yl-propionamide

Sources & evidence

ORD record
ord-7f27e898b19846ac8cb07b7c6345b860
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (7/10)
DOI
10.1039/C8SC04228D

Reaction notes

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On this pageParticipantsSources & evidenceReaction notes