HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 386622Generated: October 31, 2026
tert-Butoxy bis(dimethylamino)methane → HCID 57747332, compound
https://huagongshe.com/reaction/386622
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butoxy bis(dimethylamino)methane | HCID 79885 | — |
| Reactant | HCID 57747433 | HCID 57747433 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 57747332 | HCID 57747332 | 92% |
Reaction Steps
To a homogenous mixture of 4-(4-(4-bromo-2,6-dimethylphenoxy)-6-methyl-5-nitropyrimidin-2-ylamino)benzonitrile (22.71 g, 50 mmol) in DMF (300 ml) was added tert-butoxybis (dimethylamino) methane (12.39 ml, 60 mmol) over 15 minutes. The mixture was stirred at room temperature overnight. DMF was partially removed. The residue was washed with water and extracted with ethyl acetate (×3). The organic layers were combined, washed with brine, dried (MgSO4) and concentrated to dryness yielding to the desired product as a yellow solid (23.41 g, 46.0 mmol, 92%) which was used in next step without further purification. 1H NMR (CDCl3, 400 MHz) δ 2.14 (s, 6H), 2.98 (bs, 3H), 3.13 (bs, 3H), 5.54 (d, J=12.4 Hz, 1H), 7.03 (s, 1H), 7.27 (d, J=8.6, 2H), 7.28 (s, 2H), 7.40 (d, J=8.6, 2H), 8.03 (d, J=12.2 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08372852B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-5ad4810cd065418e90ee5f2d653b0193 |
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| Source note | uspto-grants-2013_02 |
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