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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 545002Generated: October 29, 2026

Acetic Anhydride → HCID 59851270, compound

https://huagongshe.com/reaction/545002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantDiisopropylethylamineHCID 81531—
ReactantLithium ChlorideHCID 433294—
ReactantHCID 56946380HCID 56946380—
ReactantHCID 178506946HCID 178506946—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 59851270HCID 59851270—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 2-(3,4-dimethoxy-phenylamino)-9-iodo-5H,7H-benzo[b]pyrimido[4,5-d]azepin-6-one (I-30) (0.60 g, 1.20 mmol) in dry DMF (8 mL) was added Ac2O (0.23 mL, 2.44 mmol), HCOOLi (0.19 g, 3.66 mmol), LiCl (0.155 g, 3.66 mmol), and Pd(OAc)2 (0.01 g, 0.06 mmol). Lastly, i-Pr2NEt (0.42 mL, 2.44 mmol) was added and the mixture heated for 16 h at 80° C. in a sealed tube. The reaction mixture was then diluted with CH2Cl2 (30 mL), and the organic layer was washed with H2O (3×30 mL), dried over MgSO4, filtered and concentrated in vacuo to give crude product as a yellow solid. The solid was treated with EtOAc and sonicated to provide a white solid which was collected by filtration to provide I-53 (0.33 g, 71%): HRMS Calcd. for C21H18N4O5: 407.1355, Found 407.1364.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935694B2
Source datasetuspto-grants-2011_05
ORD IDord-f3d57b05b70d44b58831dc7f56c385c2
Source noteuspto-grants-2011_05