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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1024503Generated: October 28, 2026

1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride → HCID 66726297, compound

https://huagongshe.com/reaction/1024503

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant4-(Tert-butoxycarbonyl)thiomorpholine-2-carboxylic acidHCID 2760619—
Reactant2-Amino-3,4-dimethylpyridineHCID 11007884—
ReactantN-(9-chloro-3,4-dihydro-2H-1,5-benzodioxepin-7-ylmethyl)-2-methylpropan-1-amineHCID 43087680—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 66726297HCID 66726297—

Reaction Steps

The mixture of N-(9-chloro-3,4-dihydro-2H-1,5-benzodioxepin-7-ylmethyl)-2-methylpropan-1-amine (150 mg), thiomorpholine-2,4-dicarboxylic acid 4-tert-butyl ester (137 mg), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (138 mg), and dimethyl aminopyridine (92 mg) in dichloromethane (15 ml) was stirred at room temperature overnight. After the addition of water (10 ml), the mixture was extracted with 10 ml ethyl acetate three times. The organic layer was washed with saturated sodium bicarbonate, water and brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The crude was purified by column chromatography on silica (20-33% ethyl acetate in hexane) to give the desired product as a resin: MS (m+1)=499.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722896B2
Source datasetuspto-grants-2014_05
ORD IDord-a0615283dd4243e3a2b91e33cbddf470
Source noteuspto-grants-2014_05