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Ethanesulfonyl chloride → Tert-butyl 6-cyclohexyl-3-[3-[(ethylsulfonylamino)methyl]-1,2,4-oxadiazol-5-yl]hexanoate

HRID 186039
Notes
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Reaction equation

HRID 186039 reaction equation
[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6]([CH2:7][CH:8]([CH2:9][CH2:10][CH2:11][CH:12]1[CH2:13][CH2:14][CH2:15][CH2:16][CH2:17]1)[c:18]1[n:19][c:20]([CH2:23][NH2:24])[n:21][o:22]1)=[O:25].[CH2:26]([CH3:27])[S:28](=[O:29])(=[O:30])[Cl:31]>>[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6]([CH2:7][CH:8]([CH2:9][CH2:10][CH2:11][CH:12]1[CH2:13][CH2:14][CH2:15][CH2:16][CH2:17]1)[c:18]1[n:19][c:20]([CH2:23][NH:24][S:28]([CH2:26][CH3:27])(=[O:29])=[O:30])[n:21][o:22]1)=[O:25]
ParticipantsSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 11667Ethanesulfonyl chlorideHCID 21305074Tert-butyl 3-[3-(aminomethyl)-1,2,4-oxadiazol-5-yl]-6-cyclohexylhexanoate

Product 1

HCID 21305114Tert-butyl 6-cyclohexyl-3-[3-[(ethylsulfonylamino)methyl]-1,2,4-oxadiazol-5-yl]hexanoate

Sources & evidence

ORD record
ord-8e729f0d60844b66a979165fd154c276
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (6/10)
DOI
10.1039/C8SC04228D

Reaction notes

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On this pageParticipantsSources & evidenceReaction notes