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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1926434Generated: November 1, 2026

HCID 67520656, compound → 2-[2-Amino-5-(1-piperidin-4-yl-1H-pyrazol-4-yl)-pyridin-3-yl]-benzothiazole-4-carbonitrile

https://huagongshe.com/reaction/1926434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67520656HCID 67520656—
Reactant2-Chlorobenzo[d]thiazole-4-carbonitrileHCID 67520988—
Product2-[2-Amino-5-(1-piperidin-4-yl-1H-pyrazol-4-yl)-pyridin-3-yl]-benzothiazole-4-carbonitrileHCID 67521242—

Reaction Steps

Following the procedure for 3-(7-fluoro-4-trifluoromethylbenzothiazol-2-yl)-5-(1-piperidin-4-yl-1H-pyrazol-4-yl)-pyridin-2-ylamine, using 2-chloro-1,3-benzothiazole-4-carbonitrile and conducting the Suzuki coupling at 80° C. for 2 h, the title compound was obtained as a yellow solid. 1H NMR (DMSO-d6, 400 MHz): δ=2.04-2.23 (m, 4H), 3.04 (m, 2H), 3.30 (m, 2H), 4.44 (mc, 1H), 7.59 (t, J=7.8 Hz, 1H), 7.99 (s, 1H), 8.03 (dd, J=7.6, 1.0 Hz, 1H), 8.34 (s, 1H), 8.49 (dd, J=8.1, 1.0 Hz, 1H), 8.51 (d, J=2.3 Hz, 1H), 8.86 (broad s, 1H), 9.03 (broad s, 1H). MS (ES′): m/z=402.15 [MH+]. HPLC: tR=2.28 min (ZQ3, polar—5 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178668B2
Source datasetuspto-grants-2012_05
ORD IDord-b3b3612ef3d24510951bdeb3a842cce9
Source noteuspto-grants-2012_05