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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587176Generated: October 29, 2026

4,5,6,7-Tetrahydro-3H-imidazo[4,5-c]pyridine → HCID 60197703, compound

https://huagongshe.com/reaction/587176

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,5,6,7-Tetrahydro-3H-imidazo[4,5-c]pyridineHCID 410112—
Reactant3-[(4-Chloro-1,3,5-triazin-2-yl)amino]benzenemethanesulfonamideHCID 86679822—
ProductHCID 60197703HCID 60197703—

Reaction Steps

B44 was prepared following the general procedure reported for B10 using A1 and 4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridine. The title compound (B44) was purified by reverse phase RP-HPLC (column: C18), using H2O and MeOH as eluents; yield: 34.3 mg (9%), white amorphous solid. 1H NMR (400 MHz, d6-DMSO, 300K) δ 2.59-2.71 (m, 2H), 4.07 (t, J=5.7 Hz, 2H), 4.22 (s, 2H), 4.72 (s, 2H), 6.83 and 6.89 (2 s, 2H), 7.00 (d, J=7.5 Hz, 1H), 7.29 (t, J=7.9 Hz, 1H), 7.51 (s, 1H), 7.58 and 7.65 (2 d, J=7.0 Hz and J=7.5 Hz, 1H), 7.74 and 7.88 (2 s, 1H), 8.26 (s, 1H), 9.70 (s, 1H), 11.86 (bs, 1H). MS (ES) C16H18N8O2S requires: 386. found: 387 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09226929B2
Source datasetuspto-grants-2016_01
ORD IDord-1aba4a8bead747a28ffb418c22192e96
Source noteuspto-grants-2016_01