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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1671794Generated: October 25, 2026

Hydrochloric Acid → Methyl 3-(2-fluorophenyl)-2-(2-(isopropylamino)benzo[d]thiazol-6-yl)-3-oxopropanoate

https://huagongshe.com/reaction/1671794

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzoic acid, 2-fluoro-, methyl esterHCID 67854—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantHCID 57527171HCID 57527171—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 3-(2-fluorophenyl)-2-(2-(isopropylamino)benzo[d]thiazol-6-yl)-3-oxopropanoateHCID 57527151120.2%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of lithium bis(trimethylsilyl)amide (1.0 M in THF, 15.1 mL) in THF (30 mL) was added a solution of methyl 2-(2-(isopropylamino)benzo[d]thiazol-6-yl)acetate (1.60 g, 6.05 mmol) in THF (20 mL) at −78° C. over 40 min. The resulting solution was stirred at −78° C. for 15 min before a solution of methyl 2-fluorobenzoate (1.08 mL, 8.48 mmol) in THF (10 mL) was added over 5 min. The mixture was stirred at −78° C. for 1 hr and then at rt for 3 hr before it was poured into ice-cold water (100 mL). After its pH value was adjusted to 9 with 6 N HCl, the mixture was extracted with AcOEt (3×40 mL). The combined extract was washed with brine and dried over anhydrous MgSO4. Evaporation of solvent under vacuum give the title compound (2.81 g) as an orange yellowish oil. This product was 63% pure by LCMS, but it was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994337B2
Source datasetuspto-grants-2011_08
ORD IDord-b616a649a7cd4469aac11317a0938ad8
Source noteuspto-grants-2011_08