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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175569Generated: October 30, 2026

Sodium hydride → Methyl 2-(((benzyloxy)carbonyl)(7-(trifluoromethyl)isoquinolin-1-yl)amino)acetate

https://huagongshe.com/reaction/2175569

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantMethyl bromoacetateHCID 60984—
ReactantBenzyl (7-(trifluoromethyl)isoquinolin-1-yl)carbamateHCID 58562812—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-(((benzyloxy)carbonyl)(7-(trifluoromethyl)isoquinolin-1-yl)amino)acetateHCID 58562656—

Reaction Steps

A solution of benzyl (7-(trifluoromethyl)isoquinolin-1-yl)carbamate (212 mg, 0.61 mmol), from above step F in DMF (5 mL) was cooled in an ice bath and treated with NaH (27 mg, 0.67 mmol), and the mixture was stirred for 30 min and was treated with methyl bromoacetate (64 μL, 0.67 mmol). This solution was stirred and allowed to warm to room temperature over 18 h. The reaction was quenched with saturated NH4Cl and DMF was removed under vacuum. The residue was taken in EtOAc and washed with water, sat NaCl and dried over Na2SO4. EtOAc was removed under vacuum and the residue was purified by silica column chromatography to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062048B2
Source datasetuspto-grants-2015_06
ORD IDord-b90c7c23a67f4b798e14ebbf7af08354
Source noteuspto-grants-2015_06