Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 983897Generated: October 27, 2026

Phosphorus oxychloride → HCID 67220084, compound

https://huagongshe.com/reaction/983897

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
Reactant(2-Amino-4-methoxyphenyl)(phenyl)methanoneHCID 254180—
Reactant2-Thiazolecarboxylic acid, 4-(1-methylethyl)-HCID 22499307—
SolventPyridineHCID 1049—
ProductHCID 67220084HCID 6722008456.4%

Reaction Conditions

Temperature-30 °C

Reaction Steps

Step E) To a suspension of 2.59 g (15.7 mmol) of 2-amino-4-methoxybenzophenone (product of step D) and 2.68 g (15.7 mmol) of 4-isopropylthiazole-2-carboxylic acid (product of step C) in 75 mL of pyridine cooled to −30° C., was added 1.93 mL (23.5 mmol) of POCl3 slowly dropwise over 5 min. The mixture was stirred 3 h, warmed to room temperature and was stirred overnite. The reaction mixture was poured into ice water, and extracted several times with EtOAc. The combined EtOAc extracts were dried (MgSO4), concentrated and chromatographed over SiO2 (eluted with 0% to 15% MeOH/EtOAc) to afford 2.57 g (51%) of 4-Methylthiazole-2-carboxylic acid (2-acetyl-5-methoxyphenyl)amide as a yellow solid: 1H NMR (500 MHz, CDCl3) δ 1.41 (d, J=6.7 Hz, 6H), 2.64 (s, 3H), 3.24 (m, 1H), 3.91 (s, 3H), 6.67 (dd, J=9, 2.5 Hz, 1H), 7.18 (s, 1H), 7.86 (d, J=9 Hz, 1H), 8.56 (d, J=2.5 Hz, 1H), 13.48 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06867185B2
Source datasetuspto-grants-2005_03
ORD IDord-8cbb0751e2fe43f897b2b89b67b23c5b
Source noteuspto-grants-2005_03