HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402955Generated: October 30, 2026
4-Amino-6-chloropyrimidine → HCID 86686852, compound
https://huagongshe.com/reaction/402955
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Amino-6-chloropyrimidine | HCID 238012 | — |
| Reactant | 2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenyl | HCID 2734217 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | (6-Bromopyridin-3-YL)(morpholino)methanone | HCID 65809001 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86686852 | HCID 86686852 | 40% |
Reaction Steps
To a stirred solution of (6-bromopyridin-3-yl)(morpholino)methanone (0.75 g, 2.78 mmol) in toluene (5 mL) was added 6-chloropyrimidin-4-amine (0.43 g, 3.33 mmol), Pd2(dba)3 (100 mg, 0.3 mmol), Davephos (157 mg, 0.4 mmol) and NaOt-Bu (848 mg, 8 mmol). The mixture was stirred at 150° C. for 13 hrs under N2. The mixture was evaporated and the residue was taken up in ethyl acetate (50 mL) and H2O (20 mL). The organic phase was washed with H2O (2×20 mL) and then brine (2×20 mL) and dried over Na2SO4. After filtration and concentration, the final product (350 mg, 40%) was obtained as yellow solid. LC-MS: 320.1 [M+H]+, tR=1.306 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08742098B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-8ecc71e327bd49ab9e1f105ee9f6ffa4 |
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| Source note | uspto-grants-2014_06 |
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