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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 361575Generated: October 31, 2026

2H-Isoindole-2-acetyl chloride, 1,3-dihydro-1,3-dioxo- → HCID 67767530, compound

https://huagongshe.com/reaction/361575

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2H-Isoindole-2-acetyl chloride, 1,3-dihydro-1,3-dioxo-HCID 81242—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 67767816HCID 67767816—
Solvent1,2-DichloroethaneHCID 11—
SolventWaterHCID 962—
ProductHCID 67767530HCID 6776753055.5%

Reaction Steps

To a solution of (3aR*,10aS*)-9-[3-(benzyloxycarbonylamino)benzyl]-2,3,3a,4,9,10a-hexahydrobenzo[b]cyclopenta[e][1,4]diazepin-10(1H)-one (1.9 g, 4.3 mmol) in 1,2-dichloroethane (50 mL) was added phthalimidoacetyl chloride (1.1 g, 4.7 mmol) at room temperature and the mixture was refluxed for 17 hours. After cooling, saturated aqueous NaHCO3 solution (30 mL) was added and the mixture was diluted with water and extracted with 2 portions of chloroform. The pooled organic layer was washed with saturated aqueous NaCl solution, dried over MgSO4, filtered, and concentrated under reduced pressure. The residue was crystallized from diethyl ether to provide 1.5 g (yield 55%) of the title compound. m.p. 224°-225° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05866567
Source datasetuspto-grants-1999_02
ORD IDord-c16cf7ef2b8046cb892b543097a87f42
Source noteuspto-grants-1999_02