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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 331507Generated: October 25, 2026

Triphenylphosphine dibromide → HCID 59472114, compound

https://huagongshe.com/reaction/331507

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphine dibromideHCID 70579—
ReactantDiisopropylethylamineHCID 81531—
ReactantTert-butyl 4-(2-(3-amino-6-bromopyrazine-2-carbonyl)hydrazinecarbonyl)benzyl(methyl)carbamateHCID 59472138—
SolventAcetonitrileHCID 6342—
ProductHCID 59472114HCID 59472114—

Reaction Steps

tert-butyl N-[[4-[[(3-amino-6-bromo-pyrazine-2-carbonyl)amino]carbamoyl]phenyl]methyl]-N-methyl-carbamate (7.66 g, 15.98 mmol) was dissolved in dry acetonitrile (114.9 mL) and cooled in an ice bath and put under a nitrogen atmosphere. Diisopropylethylamine (6.196 g. 8.350 mL, 47.94 mmol) was added via a syringe followed by dibromo(triphenyl)phosphorane (8.767 g, 20.77 mmol) portion wise. Reaction mixture started to precipitate out therefore left to stir for 45 minutes in an ice bath and isolated precipitated product by filtration as a beige powder (4.5 g). This material was then sonicated, triturated in acetonitrile, filtered and dried to give the sub-titled compound as yellow solid. (3.17 g, 40.9%). 1H NMR (400 MHz, DMSO-d6) δ 1.38-1.45 (br d, 9H), 2.80 (s, 3H), 4.45 (s, 2H), 7.48-7.51 (br s, 2H), 7.80 (br s, 2H), 8.10-8.20 (m, 2H), 8.45 (s, 1H) ppm; LC/MS m/z 463.1, 464.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877759B2
Source datasetuspto-grants-2014_11
ORD IDord-4d88a8ec8b264274b51187ea51d92d9e
Source noteuspto-grants-2014_11