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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1436962Generated: October 27, 2026

Dicyclohexylcarbodiimide → HCID 178523245, compound

https://huagongshe.com/reaction/1436962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant5,7-Dichloro-8-hydroxyquinoline-2-carboxylic acidHCID 21918190—
ReactantHCID 178478691HCID 178478691—
SolventTriethylamineHCID 8471—
ProductHCID 178523245HCID 178523245—

Reaction Steps

According to the procedure described in Example 1, 5,7-dichloro-8-hydroxyquinoline-2-carboxylic acid 19 (597 mg, 2.31 mmol), dicyclohexylcarbodiimide (483 mg, 2.31 mmol), 1-hydroxybenzotriazole hydrate (316 mg, 2.31 mmol), histamine dihydrochloride (425 mg, 2.31 mmol) and triethylamine (0.5 mL) gave, after column purification (silica gel, ethyl acetate/isopropanol/water (12:4:1)), 5,7-dichloro-8-hydroxyquinoline-2-carboxylic acid [2-(1H-imidazol-4-yl)-ethyl]-amide (PBT 1038) as a pale straw-coloured solid (276 mg, 34%). 1H NMR (DMSO-d6, 400 MHz): δ 11.40 (br, 2H), 9.74 (m, 1H), 8.64 (d, J=8.6, 1 H), 8.28 (d, J=8.6, 1 H), 7.92 (s, 1H), 7.53 (s, 1H), 6.83 (s, 1H), 3.59 (m, 2H), 2.81 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07619091B2
Source datasetuspto-grants-2009_11
ORD IDord-25facb826c394e49b5de02cbdc8faa78
Source noteuspto-grants-2009_11