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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768089Generated: October 25, 2026

Benzenesulfinic acid → 5-amino-1-(chloromethyl)-3-((5,6,7-trimethoxyindol-2-yl)carbonyl)-1,2-dihydro-3H-benz(e)indole

https://huagongshe.com/reaction/1768089

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfinic acidHCID 12057—
ReactantBicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)-HCID 18462—
ReactantSodiumHCID 5360545—
ReactantN-allyl-1-(chloromethyl)-3-[(5,6,7-trimethoxy-1H-indol-2-yl)carbonyl]-1,2-dihydro-3H-benzo[e]indol-5-amineHCID 9806196—
CatalystHCID 178418397HCID 178418397—
SolventDichloromethaneHCID 6344—
Product5-amino-1-(chloromethyl)-3-((5,6,7-trimethoxyindol-2-yl)carbonyl)-1,2-dihydro-3H-benz(e)indoleHCID 39170080%

Reaction Steps

Benzenesulfinic acid, sodium salt (25 mg, 0.15 mmol) and camphorsulfonic acid (40 mg, 0.17 mmol) were added to a solution of 10a (30 mg, 0.059 mmol) in dichloromethane (5 mL). Pd(Ph3P)4 (5 mg, 0.004 mmol) was added and the reaction mixture was stirred at an ambient temperature for 30 min. The mixture was purified directly via a silica gel column. Elution with EtOAc/petroleum ether (1:1) gave 1-(chloromethyl)-3-[(5,6,7-trimethoxy-1H-indol-2-yl)carbonyl]-1,2-dihydro-3H-benzo[e]indol-5-amine (11a) (22 mg, 80%), spectroscopically identical to an authentic sample (Atwell et al., J. Org Chem., 1998, 63, 9414).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07235578B2
Source datasetuspto-grants-2007_06
ORD IDord-8b7c7778a33449fcb86436e46f8aedca
Source noteuspto-grants-2007_06