Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 751536Generated: October 31, 2026

Dimethylamine → HCID 69271636, compound

https://huagongshe.com/reaction/751536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantHCID 69270149HCID 69270149—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 69271636HCID 69271636—

Reaction Conditions

Temperature60 °C

Reaction Steps

Dissolve 3-(5-methoxybenzofur-7-yl)-4-[1-(3-hydroxypropyl)-1H-indol-3-yl]pyrrole-2,5-dione (0.058 g, 0.118 mmol) in 10 mL dichloromethane. Add carbon tetrabromide (0.077 g, 1 equivalent) and triphenyl phosphine (0.061 g, 1 equivalent). Stir for 10 min, add another equivalent of both reagents. Stir 10 min then dilute with dichloromethane and wash with water followed by brine. Dry over magnesium sulfate then filter and concentrate. Purification by column chromatography (2% methanol:dichloromethane) affords the 3-(5-methoxybenzofur-7-yl)-4-[1-(3-bromopropyl)-1H-indol-3-yl)pyrrole-2,5-dione. 3-(5-Methoxybenzofur-7-yl)-4-[1-(3-bromopropyl)-1H-indol-3-yl]pyrrole-2,5-dione is dissolved in 1.5 mL 1-methyl-2-pyrrolidinone and add dimethylamine (2M solution in tetrahydrofuran, 0.3 mL, 5 equivalents). Heat to 60° C. for 16 hrs. Extract with ethyl acetate versus water, concentrate organic layer. Redissolve in a minimal amount of methanol and load onto an SCX™ Varian column (pretreated with a 5% acetic acid: methanol solution). Wash with methanol and ethyl acetate to remove impurities, flush with 2M ammonia methanol to recover product. ES(M++H)444.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07405305B2
Source datasetuspto-grants-2008_07
ORD IDord-80e62deff1614fbf8c5297e2440dd2d0
Source noteuspto-grants-2008_07