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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509875Generated: October 29, 2026

HCID 178522184, compound → 4-(4-{4-[(2-Phenyl-5-trifluoromethyl-oxazole-4-carbonyl)-amino]-phenyl}-[1,4]diazepane-1-carbonyl)-cyclohexanecarboxylic acid

https://huagongshe.com/reaction/1509875

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178522184HCID 178522184—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product4-(4-{4-[(2-Phenyl-5-trifluoromethyl-oxazole-4-carbonyl)-amino]-phenyl}-[1,4]diazepane-1-carbonyl)-cyclohexanecarboxylic acidHCID 4462885140%

Reaction Steps

Cis-4-(4-{4-[(2-Phenyl-5-trifluoromethyl-oxazole-4-carbonyl)-amino]-phenyl}-[1,4]diazepane-1-carbonyl)-cyclohexanecarboxylic acid benzyl ester (90 mg) was diluted in 30 mL of methanol and 100 mg of Pd/C (10%) was added. The mixture was placed on a Parr shaker for hydrogenation at 50 psi for 3 hr. The mixture was filtered and the solvent was removed to afford the product 4-(4-{4-[(2-phenyl-5-trifluoromethyl-oxazole-4-carbonyl)-amino]-phenyl}-[1,4]diazepane-1-carbonyl)-cyclohexanecarboxylic acid (30 mg, 40% yield) as a white solid. LCMS for C30H31F3N4O5 calcd. (m/e) 584, observed 585 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08211884B2
Source datasetuspto-grants-2012_07
ORD IDord-7b5a1ef3b64a47558dd2b0e8db297056
Source noteuspto-grants-2012_07