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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587174Generated: October 29, 2026

1,2,3,4-Tetrahydroquinoline → HCID 60197701, compound

https://huagongshe.com/reaction/587174

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2,3,4-TetrahydroquinolineHCID 69460—
Reactant3-[(4-Chloro-1,3,5-triazin-2-yl)amino]benzenemethanesulfonamideHCID 86679822—
ProductHCID 60197701HCID 60197701—

Reaction Steps

B42 was prepared following the general procedure reported for B10 using A1 and 1,2,3,4-tetrahydroquinoline; yield: 11.9 mg (3%), colorless amorphous solid. 1H NMR (400 MHz, d6-DMSO, 300K) δ 1.91 (quint, J=6.3 Hz, 2H), 2.73 (t, J=6.6 Hz, 2H), 3.98 (t, J=6.2 Hz, 2H), 4.16 (s, 2H), 6.82 (s, 2H), 6.99 (d, J=7.6 Hz, 1H), 7.05 (t, J=7.2 Hz, 1H), 7.13-7.19 (m, 2H), 7.23 (t, J=7.8 Hz, 1H), 7.62-7.69 (m, 2H), 7.72 (d, J=7.8 Hz, 1H), 8.32 (s, 1H), 9.81 (s, 1H). MS (ES) C19H20N6O2S requires: 396. found: 397 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09226929B2
Source datasetuspto-grants-2016_01
ORD IDord-8836583ff54d4f4ab3938b2187e791ab
Source noteuspto-grants-2016_01