HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249655Generated: October 27, 2026
Ammonia → 5,6-Dichloro-2-cyclopropylpyrimidine-4-carboxylic acid
https://huagongshe.com/reaction/249655
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 5-Chloro-2-cyclopropyl-1,6-dihydro-6-oxo-4-pyrimidinecarboxylic acid | HCID 136057764 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5,6-Dichloro-2-cyclopropylpyrimidine-4-carboxylic acid | HCID 58220806 | — |
Reaction Steps
Phosphorus oxychloride (14 mL, 23 g, 0.15 mol) and 5-chloro-2-cyclopropyl-1,6-dihydro-6-oxo-4-pyrimidinecarboxylic acid (i.e. the product of Step B1 or B2) (75 g, 300 mmol) were combined and heated at 85° C. for 3 h. The reaction mixture was cooled to 30° C. and added over 30 minutes to a mixture of acetonitrile (50 mL) and ice water (80 mL), with the temperature maintained at 5-10° C. and the pH maintained in the range 1-3 by co-feeding aqueous ammonia (28%). The pH was adjusted to about 2, the mixture was concentrated at 25° C. with a rotary evaporator to remove acetonitrile, and the precipitated product was isolated by filtration and washed with water (2×25 mL). The solid was dried in a vacuum oven to afford the title compound (ca. 7.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07863220B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-e706e34adbfd42c5aa7543492c59f71d |
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| Source note | uspto-grants-2011_01 |
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