HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 980370Generated: October 30, 2026
Dicyclohexylcarbodiimide → HCID 178516326, compound
https://huagongshe.com/reaction/980370
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Methanol--water (1/1) | HCID 22242641 | — |
| Reactant | HCID 178511788 | HCID 178511788 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178516326 | HCID 178516326 | — |
Reaction Steps
In 30 ml of dichloromethane was suspended 455 mg of compound (2) and after adding thereto 801 mg of HOBT and 1.059 g of DCC and stirring the mixture for 15 minutes, the reaction was maintained for 15 minutes at room temperature. The reaction mixture was ice-cooled again and then 50 ml of a dichloromethane solution of foregoing compound (11) was added to the reaction mixture. After reacting the mixture for one hour under ice-cooling, the reaction was maintained overnight at room temperature. Precipitates thus formed was filtered off and the filtrate was concentrated to dryness. The residue thus obtained was dissolved in 20 ml of water-methanol (4:1) and subjected to HP-20 column chromatography. When the eluate by water-methanol (1:4) was concentrated to dryness, 1.135 g of crude Nα -[(S)-2-azetidinone-4-carbonyl]-L-histidyl-L-proline benzyl ester (12) was obtained. When the product was subjected to silica gel column chromatography again and eluted with chloroform-methanol-aqueous ammonia (40:10:1), 927 mg of the pure product (12) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04636567 |
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| Source dataset | uspto-grants-1987_01 |
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| ORD ID | ord-3b2325f2813648ec9f3d202b4caedf64 |
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| Source note | uspto-grants-1987_01 |
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