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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 708821Generated: October 30, 2026

Phosgene → tert-Butyl N-[6-({7-bromo-15,15-difluoro-4,17,20-trimethyl-3,12-dioxo-13-oxa-4,11-diazatricyclo[14.2.2.16,10]henicosa-1(18),6,8,10 (21),16,19-hexaen-2-yl}amino)isoquinolin-1-yl]-N-[(tert-butoxy)carbonyl]carbamate

https://huagongshe.com/reaction/708821

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosgeneHCID 6371—
Reactanttert-Butyl N-{6-[({[(5-amino-2-bromophenyl)methyl](methyl)carbamoyl}[4-(1,1-difluoro-2-hydroxyethyl)-3,5-dimethylphenyl]methyl)amino]isoquinolin-1-yl}-N-[(tert-butoxy)carbonyl]carbamateHCID 118098688—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
Producttert-Butyl N-[6-({7-bromo-15,15-difluoro-4,17,20-trimethyl-3,12-dioxo-13-oxa-4,11-diazatricyclo[14.2.2.16,10]henicosa-1(18),6,8,10 (21),16,19-hexaen-2-yl}amino)isoquinolin-1-yl]-N-[(tert-butoxy)carbonyl]carbamateHCID 11809868959.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4A (289 mg, 0.362 mmol) in dichloromethane (5 mL) and acetonitrile (5.00 mL) at 0° C., was added phosgene (20% in toluene) (0.242 mL, 0.488 mmol). The reaction mixture was stirred at 0° C. for 15 min. Nitrogen was bubbled though the mixture for 0.5 h, then DMPU (˜0.4 mL) was added. The resulting solution was added dropwise via a syringe pump into a solution of TEA (0.353 mL, 2.53 mmol) in dichloromethane (90 mL) at rt over 4 h, stirred for an additional 15 min and then evaporated. The crude product was purified by flash chromatography to give 4B (177 mg, 0.215 mmol, 59.3% yield) as a white solid. MS and 1H NMR are consistent with the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174974B2
Source datasetuspto-grants-2015_11
ORD IDord-10c1514a7fa4439f8372f467f42b8d13
Source noteuspto-grants-2015_11