Hydrochloric Acid → HCID 178469979, compound

HRID 578925Notes

Reaction equation

[NH:1]([C:3]1[CH:18]=[CH:17][C:6]([C:7]([NH:9][CH2:10][CH:11]2[CH2:16][CH2:15][O:14][CH2:13][CH2:12]2)=[O:8])=[CH:5][N:4]=1)[NH2:2].C(=O)([O-])[O-].[K+].[K+].C([O:27][CH:28]=[C:29]([C:35](OCC)=O)[C:30]([O:32][CH2:33][CH3:34])=[O:31])C.Cl>O>[OH:27][C:28]1[N:1]([C:3]2[CH:18]=[CH:17][C:6]([C:7](=[O:8])[NH:9][CH2:10][CH:11]3[CH2:16][CH2:15][O:14][CH2:13][CH2:12]3)=[CH:5][N:4]=2)[N:2]=[CH:35][C:29]=1[C:30]([O:32][CH2:33][CH3:34])=[O:31]

Participants

Conditions

Temperature: 100 °C

Procedure

Combined 6-hydrazinyl-N-((tetrahydro-2 H-pyran-4-yl)methyl)nicotinamide (1.0 g, 4.00 mmol) and potassium carbonate (2.209 g, 15.98 mmol) in water (25 mL) and added diethyl 2-(ethoxymethylene)malonate (0.807 mL, 4.00 mmol) at 23° C. The reaction mixture was stirred at 100° C. for 14 hours, then 3N HCl (10 mL, 7.5 eq) was added to give a tan suspension. The solid was filtered, rinsed with water (3×5 mL), and dried in vacuo to give the title compound (1.114 g, 74.5% yield) as a yellow solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.15-1.24 (m, 2 H) 1.26 (t, J=7.07 Hz, 3 H) 1.56-1.68 (m, 2 H) 1.81 (qdd, J=11.16, 11.16, 11.16, 6.95, 3.79 Hz, 1 H) 3.19 (t, J=6.32 Hz, 2 H) 3.27 (td, J=11.75, 2.02 Hz, 2 H) 3.82-3.90 (m, 2 H) 4.18 (q, J=7.24 Hz, 2 H) 8.12 (br. s., 1 H) 8.13-8.24 (m, 1 H) 8.46 (dd, J=8.84, 2.27 Hz, 1 H) 8.76 (t, J=5.68 Hz, 1 H) 8.89 (dd, J=2.27, 0.76 Hz, 1 H) 13.73 (br. s., 1H). MS m/z [M+H]+ 329.3, 375.4.

Workup

customto give a tan suspension
filtrationThe solid was filtered
washrinsed with water (3×5 mL)
customdried in vacuo

Sources & evidence

ORD record: ord-e203a518410242fc8fc4c6ceb388385a
Source dataset: uspto-grants-2015_05
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US09040522B2

Reaction notes

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