Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158229Generated: November 1, 2026

Tert-Butylamine → 2-tert-Butylamino-4-[trimethylsilylethynyl]pyrimidine

https://huagongshe.com/reaction/1158229

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-ButylamineHCID 6385—
Reactant2-Chloro-4-(2-(trimethylsilyl)ethynyl)pyrimidineHCID 11572023—
Product2-tert-Butylamino-4-[trimethylsilylethynyl]pyrimidineHCID 12165233—

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807832B2
Source datasetuspto-grants-2010_10
ORD IDord-b49680ac1e2241cba7a48d34a48cd047
Source noteuspto-grants-2010_10