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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 969676Generated: October 27, 2026

Diisopropylethylamine → 7-{2-[(2-methoxy-pyridin-4-ylmethyl)-amino]-benzoylamino}-4,4-dimethyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/969676

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
ReactantTert-butyl 7-amino-4,4-dimethyl-3,4-dihydroisoquinoline-2(1H)-carboxylateHCID 21959561—
Reactant2-[(2-Methoxy-pyridin-4-ylmethyl)-amino]-benzoic acidHCID 62989484—
SolventDichloromethaneHCID 6344—
Product7-{2-[(2-methoxy-pyridin-4-ylmethyl)-amino]-benzoylamino}-4,4-dimethyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl esterHCID 69510784—

Reaction Steps

A mixture of 2-[(2-methoxy-pyridin-4-ylmethyl)-amino]-benzoic acid (Step A, 516 mg, 2.0 mmol), 7-amino-4,4-dimethyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester (552 mg, 2.0 mmol), TBTU (0.706 g, 2.2 mmol), and DIEA (0.7 mL) in 30 mL of CH2Cl2 was stirred at RT for 2 h. The mixture was diluted with more CH2Cl2. The organic layer was washed with water, brine, and dried with MgSO4. The solution was filtered, condensed, and the residue was purified by flash column chromatography (0 to 30% of EtOAc in CH2Cl2) to obtain the titled compound as oil. MS (ES+): 517.2 (M+H)+. Calc'd for C30H36N4O4-516.27.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07307088B2
Source datasetuspto-grants-2007_12
ORD IDord-72d3ef7d2d9e4b1a99a395f289eb2b26
Source noteuspto-grants-2007_12