Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1926381Generated: November 1, 2026

2-Chloro-6-methoxybenzothiazole → HCID 67521563, compound

https://huagongshe.com/reaction/1926381

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-6-methoxybenzothiazoleHCID 273132—
Reactant3-(6-fluorobenzothiazol-2-yl)-5-(1-piperidin-4-yl-1H-pyrazol-4-yl)-pyridin-2-ylamineHCID 67521015—
ProductHCID 67521563HCID 67521563—

Reaction Steps

Same procedure as 3-(6-fluorobenzothiazol-2-yl)-5-(1-piperidin-4-yl-1H-pyrazol-4-yl)-pyridin-2-ylamine except using 2-chloro-6-methoxy-1,3-benzothiazole in place of 2-chloro-6-fluorobenzothiazole to afford the title compound as a yellow solid. 1H NMR (400 MHz, DMSO-d6): δ=2.10-2.30 (m, 4H), 3.04-3.17 (m, 2H), 3.41 (d, J=12.8 Hz, 2H), 3.89 (s, 3H), 4.48-4.59 (m, 1H), 7.20 (dd, J=9.1, 2.5 Hz, 1H), 7.78 (d, J=2.5 Hz, 1H), 8.03 (d, J=9.1 Hz, 1H), 8.08 (s, 1H), 8.38-8.45 (m, 2H), 8.50 (d, J=2.0 Hz, 1H). MS (ES+): m/z=407.12 [MH+]. HPLC: tR=2.13 min (ZQ2, polar—5 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178668B2
Source datasetuspto-grants-2012_05
ORD IDord-8de968e4b22e4a99b4c29ba30dab3f41
Source noteuspto-grants-2012_05