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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1824440Generated: November 1, 2026

Triethylamine → HCID 69584372, compound

https://huagongshe.com/reaction/1824440

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant2,6-Dimethyl-benzoic acid 3-amino-4-tert-butoxycarbonyl-2-oxo-butyl esterHCID 23571411—
ReactantHCID 69584313HCID 69584313—
SolventDichloromethaneHCID 6344—
ProductHCID 69584372HCID 69584372—

Reaction Steps

To a solution of 6-[(naphthalene-2-carbonyl)-amino]-5-oxo-1,2,3,5,6,7,10,10a-octahydro-pyrrolo[1,2-a]azocine-3-carboxylic acid, (124 mg, 0.33 mmol)in dichloromethane is added EDCI (191 mg, 1 mmol), 2,6-dimethyl-benzoic acid 3-amino-4-tert-butoxycarbonyl-2-oxo-butyl ester, 111, (200 mg, 0.62 mmol), and triethylamine (150 ul). After consumption of the starting material, the reaction is washed with 1N HCl (1×50 ml), water (1×50 ml), and brine (1×50 ml). The CHCl2 is reduced in vacuo. The residue is used directly in the next step without purification. ESI MS 696.1 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07041696B2
Source datasetuspto-grants-2006_05
ORD IDord-fec5b9e3aa1d47a79127774db1d5d37f
Source noteuspto-grants-2006_05