1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride → HCID 86682244, compound

HRID 1428374Notes

Reaction equation

[Cl:1][C:2]1[C:6]([NH:7][CH2:8][C:9]#[CH:10])=[CH:5][N:4]([C:11]2[CH:12]=[N:13][CH:14]=[CH:15][CH:16]=2)[N:3]=1.Cl.C(N=C=NCCCN(C)C)C.[F:29][C:30]([F:39])([F:38])[CH:31]([S:36][CH3:37])[CH2:32][C:33](O)=[O:34]>CN(C)C1C=CN=CC=1.ClCCCl>[Cl:1][C:2]1[C:6]([N:7]([CH2:8][C:9]#[CH:10])[C:33](=[O:34])[CH2:32][CH:31]([S:36][CH3:37])[C:30]([F:39])([F:38])[F:29])=[CH:5][N:4]([C:11]2[CH:12]=[N:13][CH:14]=[CH:15][CH:16]=2)[N:3]=1

Participants

Conditions

Temperature: 25 °C

Procedure

To a 7 mL vial was added 3-chloro-N-(prop-2-yn-1-yl)-1-(pyridin-3-yl)-1H-pyrazol-4-amine (140 mg, 0.6 mmol), N,N-dimethylpyridin-4-amine (249 mg, 2.040 mmol), N1-((ethylimino)methylene)-N3,N3-dimethylpropane-1,3-diamine hydrochloride (276 mg, 1.440 mmol) followed by 4,4,4-trifluoro-3-(methylthio)butanoic acid (158 mg, 0.840 mmol) and DCE (1.2 mL). The solution was stirred at 25° C. for 18 hours, the crude reaction mixture was concentrated and purified with silica gel chromatography (0-100% EtOAc/hexane) to give the title compound as a brown oil (237 mg, 0.588 mmol, 98%): (IR thin film) 1674 cm−1; 1H NMR (400 MHz, CDCl3) δ 8.97 (d, J=2.6 Hz, 1H), 8.64 (dd, J=4.7, 1.3 Hz, 1H), 8.13 (s, 1H), 8.07 (ddd, J=8.3, 2.7, 1.5 Hz, 1H), 7.48 (ddd, J=8.3, 4.8, 0.5 Hz, 1H), 4.39 (s, 2H), 3.76 (dqd, J=17.2, 8.6, 3.6 Hz, 1H), 2.67 (dd, J=16.6, 3.6 Hz, 1H), 2.46 (dd, J=16.5, 9.9 Hz, 1H), 2.29 (d, J=2.5 Hz, 4H); ESIMS m/z 403 ([M+H]+).

Workup

customthe crude reaction mixture
concentrationwas concentrated
custompurified with silica gel chromatography (0-100% EtOAc/hexane)

Sources & evidence

ORD record: ord-c5271b9c97e84b559a94109f98c79ccd
Source dataset: uspto-grants-2015_01
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08937083B2

Reaction notes

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