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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418688Generated: November 2, 2026

Dicyclohexylcarbodiimide → HCID 67874079, compound

https://huagongshe.com/reaction/1418688

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantN-(tert-butoxycarbonyl)glycineHCID 78288—
ReactantHCID 613105HCID 613105—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 67874079HCID 67874079—

Reaction Steps

To a suspension of N-[(1,1-dimethylethoxy)carbonyl]glycine (1.15 g, 6.6 mmol) in CH2Cl2 (50 mL) under an argon atmosphere was added 1,3-dicyclohexylcarbodiimide (1.35 g, 6.5 mmol). After stirring at room temperature for 0.5 h, (±)-7-(1-hydroxypropyl)-8-methylindolizino[1,2-b]quinolin-9(11H)-one (1.0 g, 3.3 mmol) was added followed by a few mg of 4-dimethylaminopyridine. The resulting mixture was allowed to stir at room temperature overnight and then was filtered. The filtrate was washed successively with 2.5% aqueous NaHCO3 (100 mL), 0.1N HCl (100 mL) and H2O (100 mL), dried over sodium sulfate and concentrated in vacuo. The solid residue was purified by column chromatography on silica gel eluting with a solvent gradient of 0-2% MeOH/CH2Cl2 to provide the title compound. 1H NMR (CDCl3) d 8.34 (s, 1H), 8.21 (d, J=8.8 Hz, 1H), 7.91, (d, J=8.3 Hz, 1H), 7.81, (m, 1H), 7.63, (m 1H), 7.32 (s, 1H), 5.96 (apparent br t, J=7.0 Hz, 1H), 5.25 (s, 2H), 5.03 (br s, 1H), 4.15-3.94 (m, 2H), 2.36 (s, 3H), 2.04-184 (m, 2H), 1.44 (s, 9H), 0.99 (t, J=7.4 Hz, 3H). Anal. Calcd for C26H29N3O5.1/8 H2O: C, 67.04; H, 6.33; N, 9.02. Found: C, 66.95; H, 6.54; N, 8.83.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05883255
Source datasetuspto-grants-1999_03
ORD IDord-76f94c5f0c4c4e789c0128afc75d4b99
Source noteuspto-grants-1999_03