Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428928Generated: October 31, 2026

Lithium Hexamethyldisilazide → HCID 86298931, compound

https://huagongshe.com/reaction/1428928

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantAcetamide, 2-bromo-N-methyl-N-(2-methyl-6-benzoxazolyl)-HCID 90418141—
ReactantHCID 90418704HCID 90418704—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86298931HCID 8629893174.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937178B2
Source datasetuspto-grants-2015_01
ORD IDord-b3b7106aed294b88b4ee192ffead3bd8
Source noteuspto-grants-2015_01