HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446277Generated: October 26, 2026
Potassium Carbonate → 4-methyl-N3-(3-pyrimidin-4-yl-pyridin-2-yl)-benzene-1,3-diamine
https://huagongshe.com/reaction/446277
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | 4-(2-Chloropyridin-3-yl)pyrimidine | HCID 16108974 | — |
| Reactant | 5-(Boc-amino)-2-methylaniline | HCID 24699786 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-methyl-N3-(3-pyrimidin-4-yl-pyridin-2-yl)-benzene-1,3-diamine | HCID 58396272 | — |
| Product | [4-Methyl-3-(3-pyrimidin-4-yl-pyridin-2-ylamino)-phenyl]-carbamic acid tert-butyl ester | HCID 66970434 | — |
Reaction Steps
The title compound was prepared according to the procedure described in Tetrahedron 2001, 51, 7027-7034. Pd(OAc)2 (47 mg, 0.21 mmol), and rac-BINAP (131 mg, 0.21 mmol) were stirred in toluene (12 mL) at RT for 12 minutes. This mixture was added to 4-(2-chloro-pyridin-3-yl)-pyrimidine (1.01 g, 5.24 mmol), (3-amino-4-methyl-phenyl)-carbamic acid tert-butyl ester (1.63 g, 7.34 mmol), and K2CO3 (14.5 g, 105 mmol) in toluene (40 mL). The mixture was heated overnight at 130° C. in a sealed tube. The cooled reaction was filtered through a pad of Celite, partially concentrated and the resulting solid was filtered to yield [4-methyl-3-(3-pyrimidin-4-yl-pyridin-2-ylamino)-phenyl]-carbamic acid tert-butyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08476434B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-fca376be05a349bfb7cc06a04c26b84c |
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| Source note | uspto-grants-2013_07 |
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