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Trifluoroacetic acid → HCID 178457204, compound

HRID 25597
Notes
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Reaction equation

HRID 25597 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.F[C:20](F)(F)C(O)=O.Cl[C:27]([O:29][C:30]1[CH:35]=[CH:34][C:33]([C:36]([F:39])([F:38])[F:37])=[CH:32][CH:31]=1)=[O:28].[CH2:40]([CH2:43][NH2:44])[CH:41]=C>>[F:37][C:36]([F:39])([F:38])[C:33]1[CH:34]=[CH:35][C:30]([O:29][C:27](=[O:28])[N:2]([C@H:3]2[CH2:4][CH2:5][C@H:6]([CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][N:44]([CH2:43][CH:40]=[CH2:41])[CH3:20])[CH2:7][CH2:8]2)[CH3:1])=[CH:31][CH:32]=1
ParticipantsProcedureSources & evidenceReaction notes

Participants

5

Reactant 4

HCID 6422Trifluoroacetic acidHCID 4437323-Buten-1-amineHCID 159175974-(Trifluoromethyl)phenyl carbonochloridateHCID 178484796HCID 178484796, compound

Product 1

HCID 178457204HCID 178457204, 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-trifluoromethyl-phenyl chloroformate were reacted, followed by treatment with N-allylmethylamine to yield trans-{4-[5-(Allyl-methyl-amino)-pentyl]-cyclohexyl]-methyl-carbamic acid 4-trifluoromethyl-phenyl ester, MS: 441 (MH+).

Sources & evidence

ORD record
ord-15b54e768e02409cb2b3fc5755be896d
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