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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2036206Generated: November 3, 2026

Sodium Hydroxide → (+/-)-{4-Chloro-2-[2-(2,2-dimethyl-cyclopropanecarbonyl)-1,2,3,4-tetrahydro-isoquinolin-1-yl]-phenoxy}-acetic acid

https://huagongshe.com/reaction/2036206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant2,2-Dimethylcyclopropane-1-carboxylic acidHCID 260708—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant(+/-)-[4-Chloro-2-(1,2,3,4-tetrahydro-isoquinolin-1-yl)-phenoxy]-acetic acid ethyl esterHCID 66653751—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventFormic AcidHCID 284—
SolventDimethylformamideHCID 6228—
Product(+/-)-{4-Chloro-2-[2-(2,2-dimethyl-cyclopropanecarbonyl)-1,2,3,4-tetrahydro-isoquinolin-1-yl]-phenoxy}-acetic acidHCID 66654632—

Reaction Steps

To a solution of (±)-2,2-dimethyl-cyclopropanecarboxylic acid (26 mg, 0.20 mmol, 1.0 eq.) and (±)-[4-chloro-2-(1,2,3,4-tetrahydro-isoquinolin-1-yl)-phenoxy]-acetic acid ethyl ester (73 mg, 0.20 mmol, 1.0 eq.) in DMF (2.4 mL), DMAP (37 mg, 0.30 mmol, 1.5 eq.) and N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (58 mg, 0.30 mmol, 1.5 eq.) were added. The resulting solution was stirred at r.t. for 62 hours. 1M aq. NaOH soln. (1.2 mL) was added and the solution was stirred at r.t. for 3.5 hours. Formic acid (0.2 mL) was added. The crude mixture was purified by prep. HPLC (column: Waters XBridge, 19×50 mm, 5 um, UV/MS, acidic conditions). The two racemic diastereoisomers were separated (LC-MS 3: tR (±)-dial=0.91 and tR (±)-dia2=0.93). The title compound showed: tR=0.93.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575158B2
Source datasetuspto-grants-2013_11
ORD IDord-de649edd05cf4410bcc1caac797b01e4
Source noteuspto-grants-2013_11