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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474103Generated: October 30, 2026

Toluene → HCID 178477537, compound

https://huagongshe.com/reaction/474103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant(R)-N-(2-(6-bromo-3-fluoro-4-(triethylsilyl)pyridin-2-yl)-2-hydroxypropyl)-4-nitrobenzenesulfonamideHCID 86668073—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178477537HCID 17847753779.8%

Reaction Steps

A solution of triphenylphosphine (21.55 g, 82 mmol) and (R)—N-(2-(6-bromo-3-fluoro-4-(triethylsilyl)pyridin-2-yl)-2-hydroxypropyl)-4-nitrobenzenesulfonamide (37.56 g, 69 mmol) in 510 ml THF was cooled to 4° C. A solution of diethyl azodicarboxylate in toluene (40% by weight, 38.8 g, 89 mmol) was added in a dropwise while maintaining the temperature below 10° C. The cooling bath was removed and the rm was stirred at rt for 1 h. The reaction mixture was diluted with approx. 1000 ml toluene and THF was removed by evaporation at the rotavap. The resulting toluene solution of crude product was pre-purified on a silca gel column by eluting with hexanes/5-17% EtOAc. Purest fractions were combined, evaporated and crystallized from TBME/hexane to yield 29.2 g of the title compound as white crystals. HPLC: RtH11=2.546 min; ESIMS: 530, 532 [(M+H)+, 1 Br]; 1H-NMR (400 MHz, CDCl3): 8.40 (d, 2H), 8.19 (d, 2H), 7.39 (d, 1H), 3.14 (s, 1H), 3.02 (s, 1H), 2.01 (s, 3H) 1.03-0.83 (m, 15H); α[D]-35.7° (c=0.97, DCM).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637508B2
Source datasetuspto-grants-2014_01
ORD IDord-9846bd3fbd564261b69dbac3c205bcb8
Source noteuspto-grants-2014_01