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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338510Generated: October 30, 2026

Hydrochloric Acid → 6-Chloro-5-{4-[1-(hydroxymethyl)cyclobutyl]-3-methoxyphenyl}-1H-indole-3-carboxylic acid

https://huagongshe.com/reaction/338510

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl 6-chloro-5-(4-(1-(hydroxymethyl)cyclobutyl)-3-methoxyphenyl)-1h-indole-3-carboxylateHCID 86698842—
SolventMethanolHCID 887—
SolventSodium HydroxideHCID 14798—
Product6-Chloro-5-{4-[1-(hydroxymethyl)cyclobutyl]-3-methoxyphenyl}-1H-indole-3-carboxylic acidHCID 7176609812%

Reaction Conditions

Temperature80 °C

Reaction Steps

The mixture of methyl 6-chloro-5-{4-[1-(hydroxymethyl)cyclobutyl]-3-methoxyphenyl}-1H-indole-3-carboxylate (220 mg, 0.55 mmol) in aqueous sodium hydroxide (10%, 3 mL) and methanol (5 mL) was stirred at 80° C. for 16 hours. The mixture was acidified by concentrated HCl to pH˜4 and extracted with dichloromethane. The organic phases were combined, dried over sodium sulfate, filtered, and concentrated in vacuo to give a residue, which was purified by reverse phase HPLC to give the title compound (25 mg, 12%) as a white solid. MS (AP+) 368.1 (M−H2O+H)+, 408.1 (M+Na)+. 1H NMR (500 MHz, CD3OD) δ 8.03 (s, 1H), 7.98 (s, 1H), 7.57 (s, 1H), 7.08 (d, 1H), 6.98 (d, 2H), 3.86 (s, 2H), 3.80 (s, 3H), 2.36 (m, 4H), 2.11 (m, 1H), 1.86 (m, 1H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889730B2
Source datasetuspto-grants-2014_11
ORD IDord-093ef31b7bec46589d01f843ccbab518
Source noteuspto-grants-2014_11