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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029719Generated: November 4, 2026

1-Heptanamine → HCID 53793581, compound

https://huagongshe.com/reaction/1029719

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HeptanamineHCID 8127—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 18960815HCID 18960815—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53793581HCID 53793581—

Reaction Steps

To 1-(propyl-4-pyridinylamino)-1H-indol-5-ol (2.5 g) in 50 ml tetrahydrofuran was added 1,1'-carbonyldiimidazole (1.83 g) portionwise, and the reaction was allowed to proceed for 24 hours. To this mixture was added glacial acetic acid (2.15 ml) followed by a solution of heptylamine (1.45 ml) in tetrahydrofuran which had been treated with 0.56 ml of acetic acid. The reaction mixture was then stirred for 21 hours. The mixture was diluted with water, basified with sodium bicarbonate, and extracted with ethyl acetate. The organic layer was washed with water and dried (sat. NaCl, anhy. MgSO4). After filtration, the solvent was evaporated to yield an oil (4.6 g), which was eluted with 5% methanol/dichloromethane on a silica gel column via HPLC. The desired fractions were concentrated to yield an oil (4.5 g), which was eluted with 5% methanol/dichloromethane on a silica gel column via HPLC. The desired fractions were concentrated to yield an oil (2.8 g). This material was dissolved in 50 ml of pentane/ether (1:1) and the solution was concentrated to 15 ml, whereupon crystals precipitated out of the solution. These were collected to yield a solid (1.0 g), m.p. 83°-85° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05102891
Source datasetuspto-grants-1992_04
ORD IDord-52d093b1bd684cf1bc1976028c0d2717
Source noteuspto-grants-1992_04