Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1642759Generated: November 3, 2026

Pyridine → HCID 58017531, compound

https://huagongshe.com/reaction/1642759

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
Reactant(5S)-N-[5-Chloro-2-(1H-tetrazol-1-yl)benzyl]-1-[(2R)-2-(4-fluorophenyl)-2-hydroxyacetyl]-4,5-dihydro-1H-pyrazole-5-carboxamideHCID 44537923—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 58017531HCID 5801753190.7%

Reaction Steps

To (5S)—N-[5-chloro-2-(1H-tetrazol-1-yl)benzyl]-1-[(2R)-2-(4-fluorophenyl)-2-hydroxyacetyl]-4,5-dihydro-1H-pyrazole-5-carboxamide (Example 1) (483 mg, 1.05 mmol) in dichloromethane (10 mL) was added pyridine (2 mL) and acetic anhydride (100 μL, 1.06 mmol). The mixture was stirred for 4 h. Another portion of acetic anhydride (600 μL, 6.34 mmol) and DMAP (23 mg, 0.19 mmol) was added and the mixture was stirred for another 15 h. The solvents were removed by evaporation and the residue was purified by HPLC (MeCN gradient 0 to 100% in aqueous 0.1 M NH4OAc buffer containing 5% MeCN, C8 column: 50×300 mm). The relevant fractions were collected, combined and freeze dried to give the title compound (476 mg, 90%) as a solid material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119673B2
Source datasetuspto-grants-2012_02
ORD IDord-f81735a1753e4879bd8bdc131db3abd5
Source noteuspto-grants-2012_02