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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252057Generated: November 1, 2026

N-Methylcyclohexylamine → HCID 66891527, compound

https://huagongshe.com/reaction/252057

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylcyclohexylamineHCID 7514—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium BicarbonateHCID 516892—
Reactant1,1-Dimethylethyl 5-(3-hydroxy-1-propen-1-yl)-1H-indole-1-carboxylateHCID 66891223—
SolventDichloromethaneHCID 6344—
ProductHCID 66891527HCID 66891527—
ProductHCID 66892132HCID 66892132—

Reaction Steps

To a solution 5-(3-hydroxy-propenyl)-indole-1-carboxylic acid tert-butyl ester (0.95 mg, 3.48 mmol, 1.0 eq.) and Et3N (1.8 mL, 3.0 eq.) in methylene chloride (10 mL) at 0° C. was added MsCl (0.40 mL, 1.5 eq.). The resulting mixture was stirred for 30 min and wormed to room temperature and stirred for additional 1 h. Then cyclohexyl-methyl-amine (8.3 mL, 18 eq.) was introduced and the resulting mixture was stirred over weekend, diluted with sat. NaHCO3 and the separated aqueous phase was extracted with 3×EtOAc. The combined organic phase was dried over Na2SO4, filtered and concentrated. The residue was purified by silica gel chromatography (50% EtOAc/hexanes) to give 5-(3-morpholin-4-yl-propenyl)-indole-1-carboxylic acid tert-butyl ester or similarly 6-(3-morpholin-4-yl-propenyl)-indole-1-carboxylic acid tert-butyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868002B2
Source datasetuspto-grants-2011_01
ORD IDord-4f1cd2ca911344ac87347940e5db8042
Source noteuspto-grants-2011_01