Ethylamine → HCID 178464018, compound

HRID 967181Notes

Reaction equation

HRID 967181 reaction equation
Cl[CH2:2]/[CH:3]=[CH:4]/[C@H:5]1[CH2:10][CH2:9][C@H:8]([CH2:11][CH2:12][N:13]([CH3:27])[S:14]([C:17]2[CH:22]=[CH:21][C:20]([C:23]([F:26])([F:25])[F:24])=[CH:19][CH:18]=2)(=[O:16])=[O:15])[CH2:7][CH2:6]1.[CH2:28]([NH2:30])[CH3:29]>CN(C)C(=O)C>[CH2:28]([NH:30][CH2:2]/[CH:3]=[CH:4]/[C@H:5]1[CH2:10][CH2:9][C@H:8]([CH2:11][CH2:12][N:13]([CH3:27])[S:14]([C:17]2[CH:22]=[CH:21][C:20]([C:23]([F:26])([F:25])[F:24])=[CH:19][CH:18]=2)(=[O:16])=[O:15])[CH2:7][CH2:6]1)[CH3:29]

Participants

4

Procedure

In analogy to the method described in example 12.1, trans-N-{2-[4-(3-chloro-(E)-propenyl)-cyclohexyl]-ethyl}-N-methyl-4-trifluoromethyl-benzenesulfonamide was reacted with ethylamine in N,N-dimethylacetamide at room temperature to yield trans-N-{2-[4-(3-ethylamino-(E)-propenyl)-cyclohexyl]-ethyl}-N-methyl-4-trifluoromethyl-benzenesulfonamide as colorless viscous oil, MS: 433 (MH+).

Sources & evidence

ORD record
ord-e9baf9d1c4ec4fc595d25702758349f6
Source dataset
uspto-grants-2005_10
Patent number
US06953806B2

Reaction notes

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