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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579336Generated: October 27, 2026

N,2,2,6,6-Pentamethylpiperidin-4-amine → HCID 86727157, compound

https://huagongshe.com/reaction/579336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,2,2,6,6-Pentamethylpiperidin-4-amineHCID 13657792—
Reactant2-Bromo-5-(2-fluoro-6-methoxyphenyl)-1,3,4-thiadiazoleHCID 65433308—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
SolventSodium BicarbonateHCID 516892—
ProductHCID 86727157HCID 8672715728%

Reaction Steps

A stirred solution of 2-bromo-5-(2-fluoro-6-methoxyphenyl)-1,3,4-thiadiazole (335 mg, 1.159 mmol) and N,2,2,6,6-pentamethylpiperidin-4-amine (197 mg, 1.159 mmol) in NMP (2.5 mL) was heated at 120° C. for ˜18 hours. The reaction mixture was diluted with saturated NaHCO3(aq) (30 mL), water (20 mL), and extracted with DCM (75 mL). The organic phase was separated, dried over MgSO4 and filtered. The filtrate was concentrated in vacuo to afford the crude product as a brown oil/liquid. The crude material was purified by UV directed preparative HPLC under acidic conditions (0.1% TFA), collecting at 298 nm. The product containing fractions were combined and loaded onto a 5 g SCX cartridge (pre-wet with MeOH). The cartridge was washed with MeOH (30 mL) then flushed with 7M NH3 in MeOH (20 mL). The MeOH/NH3 was removed in vacuo to afford the title compound as an orange oil (121 mg, 28% yield). LC-MS: Rt 0.88 min; MS m/z 379.4 [M+H]+; [Method A]. 1H NMR (400 MHz, DMSO-d6) δ ppm 7.49 (td, J=8.34, 6.57 Hz, 1H), 7.03 (d, J=8.59 Hz, 1H), 6.97 (t, J=9.09 Hz, 1H), 4.26-4.36 (m, 1H), 3.86 (s, 3H), 2.98 (s, 3H), 1.62 (dd, J=11.62, 2.53 Hz, 2H), 1.42 (t, J=12.13 Hz, 2H), 1.27 (br. s., 1H), 1.20 (s, 6H), 1.09 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040712B2
Source datasetuspto-grants-2015_05
ORD IDord-51fcacf28e6d4214ab607833fd52df46
Source noteuspto-grants-2015_05