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Tetrahydrofuran → N-(1-cyclohexylethyl)-3-methoxy-4-prop-2-ynoxybenzamide

HRID 682133
Notes
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Reaction equation

HRID 682133 reaction equation
[CH2:1]1[O:2][CH2:3][CH2:4][CH2:5]1.[CH3:30][CH2:31][N:32]([CH2:33][CH3:34])[CH2:35][CH3:36].[CH3:37][CH2:38][O:39][C:40](=[O:41])[CH3:42].[CH3:6][O:7][c:8]1[cH:9][c:10]([C:11](=[O:12])[Cl:13])[cH:14][cH:15][c:16]1[O:17][CH2:18][C:19]#[CH:20].[CH:21]1([CH:27]([CH3:28])[NH2:29])[CH2:22][CH2:23][CH2:24][CH2:25][CH2:26]1>>[CH3:6][O:7][c:8]1[cH:9][c:10]([C:11](=[O:12])[NH:29][CH:27]([CH:21]2[CH2:22][CH2:23][CH2:24][CH2:25][CH2:26]2)[CH3:28])[cH:14][cH:15][c:16]1[O:17][CH2:18][C:19]#[CH:20]
ParticipantsSources & evidenceReaction notes

Participants

6

Reactant 5

HCID 8028TetrahydrofuranHCID 8471TriethylamineHCID 8857Ethyl AcetateHCID 1107331-CyclohexylethylamineHCID 574456713-Methoxy-4-(2-propynyloxy)benzoyl chloride

Product 1

HCID 57701173N-(1-cyclohexylethyl)-3-methoxy-4-prop-2-ynoxybenzamide

Sources & evidence

On this pageParticipantsSources & evidenceReaction notes
ORD record
ord-b3095d95a3794ee89371fb52b4bed2df
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (3/10)
DOI
10.1039/C8SC04228D

Reaction notes

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