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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38093Generated: October 26, 2026

Ammonium Chloride → 3-(7-Pyridin-4-yl-pyrazolo[5,1-b]thiazol-6-yl)-phenylamine

https://huagongshe.com/reaction/38093

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium BicarbonateHCID 516892—
Reactant6-(3-Nitrophenyl)-7-pyridin-4-yl-pyrazolo[5,1-b]thiazoleHCID 67423084—
CatalystZincHCID 23994—
SolventWaterHCID 962—
Solvent1,4-Dioxane--water (1/1)HCID 21886435—
Product3-(7-Pyridin-4-yl-pyrazolo[5,1-b]thiazol-6-yl)-phenylamineHCID 6742399868.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

6-(3-Nitrophenyl)-7-pyridin-4-yl-pyrazolo[5,1-b]thiazole (410 mg, 1.272 mmol) was dissolved in a 3:1 dioxane/water mixture (8 mL). Zinc powder (333 mg, 5.094 mmol, 4 eq) and ammonium chloride (680 mg, 12.72 mmol, 10 eq) were added and the mixture was stirred at 100° C. for 2 hours. It was then diluted with water, made basic by addition of saturated aqueous NaHCO3 and extracted with ethyl acetate (3×20 mL). Combined organic layers were washed with sat. aq. NaHCO3 and brine, dried over Na2SO4 and concentrated under reduced pressure. The crude product was purified by chromatography on silica gel (DCM/MeOH 97:3) to give 255 mg (68%) of 3-(7-pyridin-4-yl-pyrazolo[5,1-b]thiazol-6-yl)-phenylamine as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524707B2
Source datasetuspto-grants-2013_09
ORD IDord-d67425bcdd5e47818c01ea2b655a50cc
Source noteuspto-grants-2013_09