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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803548Generated: October 31, 2026

3-(Trifluoromethoxy)benzylamine → 4-chloro-7-(3-trifluoromethoxy-benzylamino)-2H-phthalazin-1-one

https://huagongshe.com/reaction/1803548

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethoxy)benzylamineHCID 145264—
ReactantBinap, (A+-)-HCID 634876—
ReactantSodium t-butoxideHCID 23676156—
Reactant6-Bromo-4-chlorophthalazin-1(2H)-oneHCID 53308487—
Reactant7-bromo-4-chloro-2H-phthalazin-1-oneHCID 67416999—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventEthyl AcetateHCID 8857—
SolventDimethylacetamideHCID 31374—
Product4-chloro-7-(3-trifluoromethoxy-benzylamino)-2H-phthalazin-1-oneHCID 58447315—

Reaction Steps

A mixture 6-bromo-4-chloro-2H-phthalazin-1-one and 7-bromo-4-chloro-2H-phthalazin-1-one (150 mg, 0.58 mmol), 3-(trifluoromethoxy)benzylamine (0.08 mL, 0.636 mmol), Pd2(dba)3 (61 mg, 0.0667 mmol), rac-BINAP (120 mg, 0.193 mmol) and NaOt-Bu (155 mg, 1.613 mmol) in DMA (8 mL) was heated at 80° C. for 1 h. The mixture was allowed to cool. The mixture was allowed to cool, diluted with EtOAc and washed with water. The organic layer was washed with sat.aq. NaHCO3, brine and dried (Na2SO4). Chromatography on silica (EtOAc/hexanes) afforded 4-chloro-7-(3-trifluoromethoxy-benzylamino)-2H-phthalazin-1-one (28 mg) as an off white solid, 1H (600 MHz, CDCl3) δ: 4.50 (s, 2H), 7.06 (dd, 1H), 7.14 (d, 1H), 7.18 (s, 1H), 7.28 (d, 1H), 7.38 (t, 1H), 7.44 (d, 1H), 7.78 (d, 1H), 9.48 (s, 1H), m/z (M+1) 369.93; 4-chloro-6-(3-trifluoromethoxy-benzylamino)-2H-phthalazin-1-one (22 mg) as an off white solid, 1H (600 MHz, CDCl3) δ: 4.41 (s, 2H), 6.83 (d, 1H), 6.98 (dd, 1H), 7.08 (bd, 1H), 7.16 (bs, 1H), 7.25 (s, 1H), 7.32 (t, 1H), 8.06 (d, 1H), 10.15 (s, 1H) ppm. m/z (M+1) 369.93.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349836B2
Source datasetuspto-grants-2013_01
ORD IDord-653c5837da534c2d8a2d6f8096dc81f2
Source noteuspto-grants-2013_01