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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2068712Generated: November 5, 2026

Sodium Hydroxide → 6-Bromo[1,3]thiazolo[5,4-b]pyridin-2-amine

https://huagongshe.com/reaction/2068712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantN-(6-Bromothiazolo[5,4-b]pyridin-2-yl)benzamideHCID 11002134—
SolventSulfuric AcidHCID 1118—
Product6-Bromo[1,3]thiazolo[5,4-b]pyridin-2-amineHCID 4461277498%

Reaction Steps

A solution of N-(6-bromothiazolo[5,4-b]pyridin-2-yl)benzamide III (2.0 g, 5.98 mmol) in 70% H2SO4 (10.0 mL) was heated to 140° C. for 1 h. After the completion of the reaction (TLC monitoring), the reaction mixture was poured onto crushed ice, basified with 30% aqueous NaOH solution till pH 8.0 and extracted with EtOAc (3×150 mL). The combined organics was washed with brine, dried (Na2SO4), filtered and concentrated under reduced pressure to obtain the desired product (1.34 g, 98%). 1H NMR (400 MHz, DMSO-d6): δ 7.85 (d, J=2.0 Hz, 1H), 8.05 (br s, 2H) and 8.18 (d, J=2.0 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299065B2
Source datasetuspto-grants-2012_10
ORD IDord-17fc1aa22e424997bb1c4c379aafca86
Source noteuspto-grants-2012_10