HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428928Generated: October 31, 2026
Lithium Hexamethyldisilazide → HCID 86298931, compound
https://huagongshe.com/reaction/1428928
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | Acetamide, 2-bromo-N-methyl-N-(2-methyl-6-benzoxazolyl)- | HCID 90418141 | — |
| Reactant | HCID 90418704 | HCID 90418704 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86298931 | HCID 86298931 | 74.4% |
Reaction Steps
A 0° C. solution of 4-(3-fluorophenyl)-7-methoxyphthalazin-1(2H)-one (7.0 g, 25.9 mmol) in THF (160 mL) was treated with LiHMDS (1M in THF) (38 mL, 38 mmol) and stirred for 30 min. 2-Bromo-N-methyl-N-(2-methylbenzo[d]oxazol-6-yl)acetamide (7.33 g, 25.9 mmol) in THF (40 mL) was added dropwise and stirring was maintained at rt for 16 h. The reaction mixture was diluted with water (200 mL) and the product extracted with EtOAc (3×150 mL). The organics were washed with brine (100 mL), dried over Na2SO4, and concentrated. The crude was triturated with MeOH (250 mL) to yield 2-(4-(3-fluorophenyl)-7-methoxy-1-oxophthalazin-2(1H)-yl)-N-methyl-N-(2-methylbenzo[d]oxazol-6-yl)acetamide (9.1 g, 74%). (472.87 [M+H]) 1H NMR: (400 MHz, DMSO) δ: 2.62 (s, 3H), 3.33 (s, 3H), 4.95 (s, 3H), 4.73 (s, 2H), 7.37-7.43 (m, 4H), 7.48-7.51 (d, J=2.4, 8.8, 1H), 7.58-7.73 (m, 4H), 7.90 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08937178B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-b3b7106aed294b88b4ee192ffead3bd8 |
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| Source note | uspto-grants-2015_01 |
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