HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1645291Generated: October 31, 2026
Tert-Butylamine → 2-tert-Butylamino-4-[trimethylsilylethynyl]pyrimidine
https://huagongshe.com/reaction/1645291
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | 2-Chloro-4-(2-(trimethylsilyl)ethynyl)pyrimidine | HCID 11572023 | — |
| Product | 2-tert-Butylamino-4-[trimethylsilylethynyl]pyrimidine | HCID 12165233 | — |
Reaction Steps
A mixture of 2-chloro-4-[trimethylsilylethynyl]pyrimidine (25 g, 0.12 mol) and tert-butylamine (100 mL) was heated to 80° C. for 2 d in a sealed tube. The mixture was cooled to rt and triturated with hexanes (100 mL). The resulting white precipitate was filtered and washed with hexanes. The filtrate was concentrated to give the crude product as a brown oil, which was used in the following reaction without further purification. TLC: Rf=0.40. mp 71-73° C. IR: 3293 (br, w), 2962 (w), 1569 (s). 1H NMR: 8.22 (d, J=5.0 Hz, 1H), 6.57 (d, J=5.0 Hz, 1H), 5.19 (s, 1H), 1.42 (s, 9H), 0.26 (s, 9H). 13C NMR: 162.38, 158.15, 150.95, 112.94, 102.77, 97.62, 51.41, 29.25, −0.11. Anal. Calcd for C13H21N3Si: C, 63.11; H, 8.56; N, 16.98. Found: C, 63.20; H, 8.52; N, 16.70.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08124765B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-13092b12eafb43be912221f96b203a97 |
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| Source note | uspto-grants-2012_02 |
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