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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 887678Generated: October 31, 2026

2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenyl → 7-{[2-(isoquinolin-7-ylamino)-pyridine-3-carbonyl]-amino}-4,4-dimethyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/887678

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 2734217—
ReactantIsoquinolin-7-amineHCID 14660277—
Reactant7-[(2-Chloro-pyridine-3-carbonyl)-amino]-4,4-dimethyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl esterHCID 86603238—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
Product7-{[2-(isoquinolin-7-ylamino)-pyridine-3-carbonyl]-amino}-4,4-dimethyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl esterHCID 68799969—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a mixture of 7-[(2-chloro-pyridine-3-carbonyl)-amino]-4,4-dimethyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester (20.8 g, 50 mmol, 1.0 eq.), 7-aminoisoquinoline (7.2 g, 50 mmol, 1.0 eq.), Pd2(dba)3 (915 mg, 1 mmol, 0.02 eq), 2-dicyclohexylphosphino-2′-(N,N-dimethylamino)biphenyl (CAS#213697-53-1, Strem Chemicals cat no. 15-1145; 785 mg, 2 mmol, 0.04 eq) under N2 in a 250 mL pressure reaction vessel was added 1.0 M LiNTMS2 THF solution (120 mL, 120 mmol, 2.4 eq.). The reaction vessel was sealed with a Teflon screwcap and the mixture was stirred at 70° C. for 17 h. The mixture was then cooled to RT. 100 mL of water was added to the mixture and the mixture was extracted with 500 mL of EtOAc. The organic layer was washed with sat. NH4Cl solution, 1M NaHPO4 solution (4×200 mL) then dried over MgSO4. After filtration and concentration, the crude was purified through a silica gel column chromatography, eluting with CH2Cl2/EtOAc. The desired title compound was obtained as a yellow solid. MS (ES+): 524 (M+H)+. Calc'd for C31H33N5O3—523.26

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247430B2
Source datasetuspto-grants-2012_08
ORD IDord-0c0ad855cf5041d18931fbffaa26a888
Source noteuspto-grants-2012_08