HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1891040Generated: October 31, 2026
Hydrochloric Acid → HCID 178507161, compound
https://huagongshe.com/reaction/1891040
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1,3-Dichloro-2-isocyanatobenzene | HCID 604537 | — |
| Reactant | 4-Amino-2-chloropyrimidine-5-carbonitrile | HCID 2801166 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178507161 | HCID 178507161 | 57.1% |
Reaction Steps
1.12 g of sodium hydride was added to an N,N-dimethylformamide (35 mL) solution containing 3.0 g of 4-amino-2-chloropyrimidin-5-carbonitrile, and the mixture was stirred for 5 minutes at room temperature. Then, 4.38 g of 2,6-dichlorophenyl isocyanate was added to the reaction mixture, which was then stirred for 1 hour at room temperature. Thereafter, ethyl acetate and a 1 N hydrochloric acid aqueous solution were added to the reaction mixture to separate the organic layer. After washing with saturated saline, the solution was dried with anhydrous magnesium sulfate, and the solvent was distilled away. The deposited solid was solidified using a methanol-ethyl acetate mixed solvent. After leaching, 3.8 g of a white solid was obtained as a subject compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08507505B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-44fb22245fd14b39af6af0a33b3ed4f7 |
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| Source note | uspto-grants-2013_08 |
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