HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375317Generated: November 1, 2026
Dicyclohexylcarbodiimide → HCID 86587853, compound
https://huagongshe.com/reaction/1375317
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Reactant | HCID 86587851 | HCID 86587851 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86587853 | HCID 86587853 | 71% |
Reaction Steps
N-Hydroxysuccinimide (12 mg, 0.10 mmol) and 2,6-dibromo-4-(2-carboxyethyl)phenyl acridine-9-carboxylate (50 mg, 0.090 mmol) were dissolved in anhydrous DMF (3 ml) and cooled to −20° C. Dicyclohexylcarbodiimide (DCC, 22 mg, 0.11 mmol) was added and the mixture was stirred at −20° C. for 2 h. The solution was stirred overnight at room temperature, and then evaporated to dryness. The residue was extracted with dichloromethane (50 ml) and the filtrate was evaporated to obtain the crude product (100 mg). Further purification was carried out by chromatotron, eluted with chloroform. The solvent was evaporated from the appropriate combined fractions to give the desired product as a light-brown solid (40 mg, 64%), mp 175–6° C. FAB-MS m/z 627 [(M+1)+, 20%], 225 [100], 206 [18], 179 [10], 143 [8].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07169554B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-a9767a0fb27c4cb58bf1b79384dee762 |
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| Source note | uspto-grants-2007_01 |
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