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Trifluoroacetic acid → HCID 178457206, compound

HRID 25608
Notes
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Reaction equation

HRID 25608 reaction equation
[CH3:1][NH:2][C@H:3]1[CH2:8][CH2:7][C@H:6]([CH2:9][CH2:10][CH2:11][CH2:12][CH2:13]OS(C)(=O)=O)[CH2:5][CH2:4]1.FC(F)(F)C(O)=O.Cl[C:27]([O:29][C:30]1[CH:35]=[CH:34][C:33]([Cl:36])=[CH:32][CH:31]=1)=[O:28].[CH3:37][NH:38][CH2:39][CH2:40][CH3:41]>>[Cl:36][C:33]1[CH:34]=[CH:35][C:30]([O:29][C:27](=[O:28])[N:2]([CH3:1])[C@H:3]2[CH2:4][CH2:5][C@H:6]([CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][N:38]([CH3:37])[CH2:39][CH2:40][CH3:41])[CH2:7][CH2:8]2)=[CH:31][CH:32]=1
ParticipantsProcedureSources & evidenceReaction notes

Participants

5

Reactant 4

HCID 6422Trifluoroacetic acidHCID 12315N-MethylpropylamineHCID 1390594-Chlorophenyl chloroformateHCID 178484796HCID 178484796, compound

Product 1

HCID 178457206HCID 178457206, compound

Procedure

In analogy to examples 29.10 and 29.11, trans-Methansulfonic acid 5-(4-methyl amino-cyclohexyl)-pentyl ester.trifluoroacetic acid salt and 4-chlorophenyl chloroformate were reacted, followed by treatment with methyl-propyl-amine to give trans-Methyl-{4-[5-(methyl-propyl-amino)-pentyl]-cyclohexyl}-carbamic acid 4-chloro-phenyl ester, MS: 409 (MH+, 1Cl).

Sources & evidence

ORD record
ord-13bbc63a3b254508995776634680eb4d
Source dataset
uspto-grants-2005_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06858651B2

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes