HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1011745Generated: October 25, 2026
Oxalyl chloride → N-(1-methyl-1H-pyrazol-3-yl)-3,5-bis[(phenylmethyl)oxy]benzamide
https://huagongshe.com/reaction/1011745
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 3,5-Bis(phenylmethoxy)benzoic acid | HCID 99307 | — |
| Reactant | 1-Methyl-3-aminopyrazole | HCID 137254 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(1-methyl-1H-pyrazol-3-yl)-3,5-bis[(phenylmethyl)oxy]benzamide | HCID 53629651 | 59.9% |
Reaction Steps
Oxalyl chloride (7.71 mL, 89.7 mmol) was added dropwise to a suspension of 3,5-dibenzyloxybenzoic acid (20.0 g, 59.8 mmol) in DCM (0.5 L) under argon. The reaction was stirred at RT for 6 hours after which time the volatiles were removed in vacuo. The residue was taken up in DCM (300 mL) and a solution of 1-methyl-1H-pyrazol-3-amine (5.81 g, 59.8 mmol) in DCM (50 mL) was added dropwise. The resulting solution was stirred for 16 hours at RT after which time a precipitate had formed. The solid was isolated by filtration and recrystallised from ethanol to give the title compound as a white solid (14.8 g). 1H NMR δ (d6-DMSO): 3.84 (3H, s), 5.17 (4H, s), 6.59 (1H, d), 6.84 (1H, t), 7.33-7.46 (12H, m), 7.62 (1H, d), 10.83 (1H, s); m/z 414 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07977328B2 |
|---|
| Source dataset | uspto-grants-2011_07 |
|---|
| ORD ID | ord-905f84f541ae4048bc4544ffc10b341b |
|---|
| Source note | uspto-grants-2011_07 |
|---|