HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 444332Generated: October 30, 2026
Dicyclohexylcarbodiimide → HCID 13134791, compound
https://huagongshe.com/reaction/444332
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 13134789 | HCID 13134789 | — |
| Reactant | Ammonia dichloromethane | HCID 22731429 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 13134791 | HCID 13134791 | 40% |
Reaction Steps
A mixture of 40 mg of (5,6-dihydro benzo[b]pyrido[3,2-f]oxepin-8-yl)-acetic acid, 60 mg of dicyclohexylcarbodiimide and 2 ml of dry dichloromethane was stirred under ice cooling. To the resulting mixture was added 8 ml of a saturated liquid ammonia-dichloromethane solution, and the mixture was stirred for 3 hours. After the completion of the reaction, this was basified with a saturated sodium hydrogen carbonate solution and extracted with ethyl acetate. The extract was washed with water and then with a saturated sodium chloride solution and dried over anhydrous sodium sulfate. The solvent was distilled off to obtain a light yellow oil, which was chromatographed over 4 g of silica gel and eluted with chloroform/ethyl acetate (10/1-8/2) to obtain crystals. These were recrystallized from ethyl acetate to yield 15 mg (yield: 40%) of (5,6-dihydro benzo[b]pyrido[3,2-f]oxepin-8-yl)-acetamide as light yellow needle crystals having a melting point of 164°-165° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04263437 |
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| Source dataset | uspto-grants-1981_04 |
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| ORD ID | ord-f5344fc7d71345ce80af81294dd89432 |
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| Source note | uspto-grants-1981_04 |
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