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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 735676Generated: October 30, 2026

PyBOP → 14-(1-(Bis(tert-butoxycarbonyl)amino)isoquinolin-6-ylamino)-2-oxa-5,12-diaza-tricyclo[13.2.2.16,10]icosa-1(18),6(20),7,9,15(19),16-hexaene-4,13-dione

https://huagongshe.com/reaction/735676

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyBOPHCID 2724699—
Reactant2-(4-(2-(3-((Benzyloxycarbonylamino)methyl)phenylamino)-2-oxoethoxy)phenyl)-2-(1-(bis(tert-butoxycarbonyl)amino)isoquinolin-6-ylamino)acetic acidHCID 57842637—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product14-(1-(Bis(tert-butoxycarbonyl)amino)isoquinolin-6-ylamino)-2-oxa-5,12-diaza-tricyclo[13.2.2.16,10]icosa-1(18),6(20),7,9,15(19),16-hexaene-4,13-dioneHCID 5784289716%

Reaction Steps

A solution of 66D (55 mg, 0.082 mmol) in 10 mL DMF was added to a solution of PyBOP (88 mg, 0.17 mmol), DMAP (49 mg, 0.4 mmol), and TEA (40 mg, 0.4 mmol) in CH2Cl2 (30 mL) dropwise through syringe pump over 3 h. The solution was stirred at rt for 16 h. The solution washed with 1M H3PO4, sat NaHCO3 and brine, dried (Na2SO4) and concentrated. The crude product was purified by flash chromatography (0 to 80% EtOAc in hexanes) to give 66F (8.5 mg, 16%). MS (ESI) m/z 654.8 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592331B2
Source datasetuspto-grants-2009_09
ORD IDord-0517fa9b27cf461e9a54cee34a23d65c
Source noteuspto-grants-2009_09