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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356800Generated: November 1, 2026

Hydrochloric Acid → HCID 7147096, compound

https://huagongshe.com/reaction/2356800

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantLithium HydroxideHCID 3939—
ReactantHCID 59385244HCID 59385244—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 7147096HCID 7147096—

Reaction Conditions

Temperature50 °C

Reaction Steps

As shown in Reaction Scheme 5, methyl 3′-fluoro-4′-[(6-fluoro-1,3-benzothiazol-2-yl)amino]biphenyl-4-carboxylate (0.64 g, 1.6 mmol) was suspended in THF (10 mL), MeOH (10 mL) and water (5 mL), and LiOH (0.39 g, 16.2 mmol) was added. The reaction mixture was heated at 50° C. until dissolution was achieved, and then the mixture was stirred for 3 days at rt. The reaction mixture was brought to pH 4 with 1N HCl and was extracted with EtOAc (3×25 mL). The combined organic phases were washed with water (2×50 mL) and brine (50 mL), dried over MgSO4, filtered, and concentrated in vacuo. This yielded 0.518 g (84%) of the desired product as an off-white solid. LC/MS m/z 383.3 (MH+), retention time 3.83 min. 1H NMR (400 MHz, DMSO-d6) δ 7.18 (t, 1H), 7.59-8.00 (m, 8H), 8.70 (t, 1H), 10.50 (bs, 1H), 12.95 (bs, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759376B2
Source datasetuspto-grants-2010_07
ORD IDord-0f773db221744e1d9a4c095fd34e1ad7
Source noteuspto-grants-2010_07