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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015349Generated: October 31, 2026

Tris(hydroxymethyl)aminomethane → HCID 25002761, compound

https://huagongshe.com/reaction/1015349

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTris(hydroxymethyl)aminomethaneHCID 6503—
Reactant4-MethylmorpholineHCID 7972—
Reactant3,4-Difluorobenzoyl chlorideHCID 2724519—
Reactant5-(Piperidin-4-ylmethoxy)quinazoline-2,4-diamineHCID 57576565—
SolventDimethylformamideHCID 6228—
ProductHCID 25002761HCID 25002761157.8%

Reaction Steps

5-(Piperidin-4-ylmethoxy)quinazoline-2,4-diamine (50 mg; 0.18 mmol) was shaken for 60 hours at room temperature in the presence of 3-(morpholino)propyl polystyrene sulfonamide (PS-NMM) (160 mg; 0.4 mmol) and 3,4-difluorobenzoyl chloride (65.3 mg; 0.37 mmol) in 4 mL N,N-dimethylformamide. Tris-(2-aminoethyl)aminomethyl polystyrene (PS-Trisamine) (112 mg; 0.4 mmol) was then added to the mixture and continued to shake for an additional 2 hours. Resins were filtered off and rinsed with methanol. Filtrate was concentrated at reduced pressure, and residue was triturated with 2 mL 1 N NaOH and ethanol (1:1). Solids were collected by filtration to yield [4-(2,4-diamino-quinazolin-5-yloxymethyl)-piperidin-1-yl]-(3,4-difluorophenyl)-methanone (117.4 mg; 76% yield). 1HNMR (400 MHz, DMSO-d6) δ 7.51 (m, 2H), 7.35 (t, J=8.4 Hz, 1H), 7.26 (m, 3H), 6.77 (d, J=8.4 Hz, 1H), 6.54 (d, J=8.4 Hz, 1H), 5.94 (br s, 2H), 4.50 (br s, 1H), 4.03 (d, J=6.0 Hz, 2H), 3.60 (br s, 1H), 3.11 (br s, 1H), 2.82 (br s, 1H), 2.22 (s, 1H), 1.87 (br s, 1H), 1.75 (br s, 1H), 1.31 (m, 2H). MS m/z (ESI) 414 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985755B2
Source datasetuspto-grants-2011_07
ORD IDord-8d587240d94b454fb00279fa22a66964
Source noteuspto-grants-2011_07