HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222068Generated: October 30, 2026
Lithium Hexamethyldisilazide → HCID 57747371, compound
https://huagongshe.com/reaction/222068
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | HCID 57747399 | HCID 57747399 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57747371 | HCID 57747371 | 95% |
Reaction Steps
To a cold mixture of tert-butyl 4-(4-bromo-2,6-dimethylphenoxy)-5H-pyrrolo[3,2-d]pyrimidin-2-yl(4-cyanophenyl)carbamate (0.81 g, 1.5 mmol) in THF (5 ml) at −78° C. was added a solution of LiHMDS (1 M, 2 ml, 2 mmol). The mixture was warmed to 0° C. over 2 hours and then was cooled to −78° C. Idomethane (0.37 ml, 6 mmol) was added and the mixture was warmed to room temperature over 2 hours and then stirred at this temperature for an additional 2 hours. The mixture was washed with brine, extracted with ethyl acetate (×3). The organic layers were combined dried over MgSO4 and concentrated to dryness. The crude material was purified by chromatography on silica to obtain the title compound (0.782 g, 1.42 mmol, 95%). 1H NMR (CDCl3, 400 MHz) δ 1.32 (s, 9H), 2.07 (s, 6H), 4.18 (s, 3H), 6.65 (d, J=3.8 Hz, 1H), 7.15 (d, J=8.8 Hz, 2H), 7.21 (s, 2H), 7.37 (d, J=3.8 Hz, 1H), 7.49 (d, J=8.8, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08207178B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-910d4609e07c4459944278a2bcf0b21d |
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| Source note | uspto-grants-2012_06 |
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