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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654438Generated: October 25, 2026

Triethylamine → Amitriptyline

https://huagongshe.com/reaction/1654438

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantN-HydroxysuccinimideHCID 80170—
ReactantST51005980HCID 2725051—
SolventDimethylformamideHCID 6228—
ProductAmitriptylineHCID 2160—

Reaction Steps

6-Carboxyfluorescein (1.00 g, 2.66 mmol) was dissolved in 8 mL DMF, 306 mg (2.66 mmol) of N-hydroxysuccinimide (HOSu) was added, 549 mg (2.66 mmol) of 1,3-dicyclohexylcarbodiimide (DCC) was added, and the reaction stirred for 17 hours, under N2, in the dark. The reaction was then vacuum filtered, filtrate combined with 784 mg (2.65 mmol) of 2-aminoimipramine (26c), 0.56 mL (4.0 mmol) of triethylamine, and 4.0 mL DMF, and reaction allowed to stir 4 days under N2, in the dark. Reaction solvents were removed in vacuo and residue purified on reverse phase C18 preparative (1 mm) TLC plates, eluting with H2O/THF/HOAc (40/60/0.4) followed by preparative HPLC on a Waters mbondapak C18 column (19 mm×150 mm), eluting with H2O/THF/HOAc (35/65/0.4) at a flow rate of 7.0 mL/minute to yield 410 mg (24%) of the desired tracer (27) as an orange powder; mass spec (FAB) (M+H)+ 654.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05407835
Source datasetuspto-grants-1995_04
ORD IDord-f2f080c2bc3648e496e1ef9e2f5f9d09
Source noteuspto-grants-1995_04