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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 980370Generated: October 30, 2026

Dicyclohexylcarbodiimide → HCID 178516326, compound

https://huagongshe.com/reaction/980370

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantMethanol--water (1/1)HCID 22242641—
ReactantHCID 178511788HCID 178511788—
SolventDichloromethaneHCID 6344—
ProductHCID 178516326HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04636567
Source datasetuspto-grants-1987_01
ORD IDord-3b2325f2813648ec9f3d202b4caedf64
Source noteuspto-grants-1987_01