HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2282942Generated: October 25, 2026
Acetonitrile → 6-Amino-2-(4-chlorophenyl)pyrimidine-4-carboxylic acid
https://huagongshe.com/reaction/2282942
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 2-(4-Chlorophenyl)-6-hydroxypyrimidine-4-carboxylic acid | HCID 135878882 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-Amino-2-(4-chlorophenyl)pyrimidine-4-carboxylic acid | HCID 46863985 | — |
Reaction Steps
To phosphorus oxychloride (180 mL) was added 2-(4-chlorophenyl)-1,6-dihydro-6-oxo-4-pyrimidinecarboxylic acid (i.e. the product of Step A) (81.81 g, 326 mmol). The mixture was heated to 90° C. for 2.5 h. After cooling to room temperature the reaction mixture was slowly added to 1:2 acetonitrile:water (1.5 L) while keeping the temperature between 35 and 45° C. After the reaction mixture was stirred at room temperature for 30 minutes the resulting solid was isolated by filtration and washed with water. The solid was then combined with aqueous ammonia (5%, 2.1 L) and heated to 80° C. for 18 h. After 2 days at room temperature the solid was isolated by filtration and washed with water. A second crop was obtained by cooling the filtrate and refiltering. The combined solids were dried to afford the title compound (58.8 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09144240B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-3eefd357afef4416b790c105dabe9d0e |
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| Source note | uspto-grants-2015_09 |
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