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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037692Generated: October 30, 2026

Dicyclohexylcarbodiimide → HCID 67434865, compound

https://huagongshe.com/reaction/1037692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant2-DimethylaminopyridineHCID 21885—
ReactantN-(tert-butoxycarbonyl)glycineHCID 78288—
ReactantHCID 46701881HCID 46701881—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67434865HCID 67434865—

Reaction Steps

56 mg of tert-butoxycarbonylaminoacetic acid, 33 mg of N,N′-dicyclohexylcarbodiimide and 2 mg of dimethylaminopyridine (DMAP) are added to a solution of 80 mg of 2-[2-amino-4-(1,3-dihydroisoindole-2-carbonyl)quinazolin-6-yl]-N-(2-hydroxyethyl)-N-methylbenzenesulfonamide in 1 ml of THF. After 120 min, the mixture is evaporated in vacuo, the residue is taken up in 1 ml of DCM:TFA (1:1) with cooling, and the mixture is stirred for 30 min. The mixture is evaporated to dryness in vacuo, the residue is taken up in 500 μl of DMSO and purified by column chromatography on a reversed phase.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546565B2
Source datasetuspto-grants-2013_10
ORD IDord-bb3fe785e187407a950f8d9f90ad0f06
Source noteuspto-grants-2013_10