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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164485Generated: October 31, 2026

Dicyclohexylcarbodiimide → HCID 131714159, compound

https://huagongshe.com/reaction/2164485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1,4-DioxaneHCID 31275—
ReactantN-HydroxysuccinimideHCID 80170—
ReactantHCID 131714160HCID 131714160—
SolventEthyl AcetateHCID 8857—
ProductHCID 131714159HCID 131714159—

Reaction Steps

A solution of Boc-Ser(tBu)-Asp(OtBu)-Ala-OH.CHA (1.205 g, 2.0 mmol) was extracted with a mixture of EtOAc: 0.5N H2SO4 (10 mL-10 mL). The organic layer was retained, washed with saturated NaCl, dried (MgSO4) and evaporated in vacuo. The resultant free acid in EtOAc:dioxane (5 mL-10 mL) was treated with HOSu (230 mg, 2.0 mmol, 1 eq) and cooled to 0°. To the cold stirring solution DCC (412 mg, 2.0 mm, 1 eq) was added portionwise and stirring proceeded at 0° for 1 hr and at 25° for 48 hr. The reaction mixture was filtered and the filtrate evaporated to dryness and crystallized from isopropanol-petroleum ether. Yield: 631 mg (52.5%); mp 129°-136°; [α]D25 -32.74° (c 1, MeOH); Rf 0.86 (CHCl3 :MeOH:AcOH; 85-10-5); Rf 0.79 (CHCl3 :MeOH:AcOH; 80-5-2). Anal. calc. for C27H44N4O11 (600.67): C, 53.99; H, 7.38; N, 9.33. Found C, 53.85; H, 7.50; N, 9.29.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04504415
Source datasetuspto-grants-1985_03
ORD IDord-2d36742cff2f40b9b9cda8dfa7c2c613
Source noteuspto-grants-1985_03