Ethylamine → HCID 11199427, compound

HRID 2240870Notes

Reaction equation

HRID 2240870 reaction equation
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([N:9]([CH2:15][C:16]([F:19])([F:18])[F:17])[C@H:10]([C:12]([OH:14])=O)[CH3:11])=[CH:5][C:4]=1[C:20]([F:23])([F:22])[F:21])#[N:2].[CH2:24]([NH2:26])[CH3:25]>>[C:1]([C:3]1[CH:8]=[CH:7][C:6]([N:9]([CH2:15][C:16]([F:18])([F:17])[F:19])[C@H:10]([C:12]([NH:26][CH2:24][CH3:25])=[O:14])[CH3:11])=[CH:5][C:4]=1[C:20]([F:22])([F:21])[F:23])#[N:2]

Participants

3

Reactant 2

HCID 6341EthylamineHCID 71413886N-[4-Cyano-3-(trifluoromethyl)phenyl]-N-(2,2,2-trifluoroethyl)-L-alanine

Product 1

HCID 11199427HCID 11199427, compound

Procedure

Synthesized as described in example 3 using N-[4-cyano-3-(trifluoromethyl)phenyl]-N-(2,2,2-trifluoroethyl)alanine and ethylamine: 1H NMR (400 MHz, CDCl3) δ 7.65 (d, J=8.8 Hz, 1H), 7.10 (d, J=2.7 Hz, 1H), 6.96 (dd, J=8.8, 2.8 Hz, 1H), 5.95 (bs, 1H), 4.26 (q, J=7.1 Hz, 1H), 4.10 (m, 2H), 3.28 (m, 2H), 1.58 (d, J=7.1 Hz, 3H), 1.06 (t, J=7.4 Hz, 3H).

Workup

  1. customSynthesized

Sources & evidence

ORD record
ord-cd767823e9fa4a42944432d52495b7f5
Source dataset
uspto-grants-2010_05
Patent number
US07723385B2

Reaction notes

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