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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1779162Generated: October 31, 2026

1H-Isoindole-1,3(2H)-dione, 2-(bromomethyl)- → HCID 131734846, compound

https://huagongshe.com/reaction/1779162

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Isoindole-1,3(2H)-dione, 2-(bromomethyl)-HCID 79244—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 90060133HCID 90060133—
SolventDichloromethaneHCID 6344—
ProductHCID 131734846HCID 13173484676%

Reaction Steps

To a mixture of No. 5317776 (Compound E; 60 mg, 0.08 mmol), DBU (19 μL, 0.126 mmol) and dichloromethane (0.84 mL) was added 2-bromomethyl-isoindole-1,3-dione (30 mg, 0.126 mmol) commercially available from Aldrich (cat. No. 252611). After the mixture was stirred at room temperature for 6 hours, further 2-bromomethyl-isoindole-1,3-dione (10 mg, 0.04 mmol) and DBU (6.3 μL, 0.04 mmol) were added. Then, 4-(1,3-dioxo-1,3-dihydro-isoindole-2-ylmethyl) 1-butyl (S)-2-{(E)-(S)-1-[(S)-2-(4-but-2-ynyloxy-phenyl)-1-methoxycarbonyl-ethylcarbamoyl]-10-oxo-heptadec-2-enyl}-2-hydroxy-succinate (56 mg, 76%) was obtained (ESI (LC/MS positive mode) m/z 873 (M+H); Rt 3.38 min.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266853B2
Source datasetuspto-grants-2016_02
ORD IDord-28157afdae9846a2917b9f6a0df3c3d4
Source noteuspto-grants-2016_02