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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820023Generated: November 2, 2026

Hydrogen Bromide → HCID 59700160, compound

https://huagongshe.com/reaction/1820023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantThioglycolic AcidHCID 1133—
ReactantHCID 67061262HCID 67061262—
SolventAcetic AcidHCID 176—
ProductHCID 59700160HCID 5970016067%

Reaction Steps

To a solution of 3-[3-(2-methoxy-phenyl)-1H-pyrrolo[2,3-b]pyridin-5-yl]-benzoic acid tert-butyl ester (1.97 g, 4.92 mmol) in acetic acid (4 mL) was added dropwise a premixed solution of hydrogen bromide (33% wt in acetic acid) (889 uL, 4.92 mmol) and mercaptoacetic acid (444 uL, 6.39 mmol). The sides of the flask were rinsed with additional acetic acid (3 mL) and the reaction solution was stirred at ambient temperature for 10 minutes whereupon the product began to precipitate out of solution. The reaction was stirred for an additional hour at ambient temperature. The precipitate was filtered and rinsed well with acetic acid and diethyl ether, affording the title compound as a bright yellow solid (448 mg, 67% yield). 1H NMR (500 MHz, d6-DMSO) δ 12.03 (br s, 1H), 8.58 (s, 1H), 8.21 (d, 2H), 7.99 (d, 1H), 7.94 (d, 1H), 7.76 (d, 1H), 7.61 (m, 2H), 7.31 (t, 1H), 7.14 (d, 1H), 7.06 (t, 1H), 3.83 (s, 3H). MS: m/e 345.1 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601839B2
Source datasetuspto-grants-2009_10
ORD IDord-e0f905be7d9248ed99e28ae975846ec8
Source noteuspto-grants-2009_10