Ammonia → HCID 67026145, compound

HRID 713817Notes

Reaction equation

[C:1]([C:3]1[CH:4]=[C:5]([CH:10]=[C:11]([F:13])[CH:12]=1)[C:6](=[N:8][OH:9])[NH2:7])#[N:2].FC1C=[C:17]([C:23]#[N:24])[CH:18]=[C:19]([CH:22]=1)[C:20]#N.C(Cl)(=O)C1C=CC=NC=1.N>>[F:13][C:11]1[CH:12]=[C:3]([CH:4]=[C:5]([C:6]2[N:7]=[C:22]([C:19]3[CH:20]=[N:24][CH:23]=[CH:17][CH:18]=3)[O:9][N:8]=2)[CH:10]=1)[C:1]#[N:2]

Participants

Reactant 4

HCID 222Ammonia

HCID 82604Nicotinoyl chloride

HCID 27830945-Fluoroisophthalonitrile

HCID 73855262HCID 73855262, compound

Product 1

HCID 67026145HCID 67026145, compound

Procedure

The title compound was prepared according to the procedure of Example 4B using 3-cyano-5-fluoro-N′-hydroxybenzimidamide (Prepared from 5-fluoroisophthalonitrile using the procedure described in Example 4A) and nicotinoyl chloride (Aldrich). 1H NMR (300 MHz, DMSO-d6) δ 7.77 (m, 1H), 8.2 (m, 2H), 8.4 (m, 1H), 8.6 (m, 1H), 8.9 (m, 1H), 9.4 (m, 1H) ppm; MS (DCl/NH3) m/z 267 (M+H)+.

Sources & evidence

ORD record: ord-5027043716d14eaaab483bd7e80ac035
Source dataset: uspto-grants-2015_11
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US09186407B2

Reaction notes

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