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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1712129Generated: October 31, 2026

Water → Phenyl (3-(benzyloxy)-4-cyanoisothiazol-5-yl)carbamate

https://huagongshe.com/reaction/1712129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyridineHCID 1049—
ReactantBromineHCID 24408—
ReactantHCID 178511143HCID 178511143—
SolventAcetonitrileHCID 6342—
ProductPhenyl (3-(benzyloxy)-4-cyanoisothiazol-5-yl)carbamateHCID 29939179—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 0° C. suspension of the adduct, 2-cyano-3-mercapto-3-phenoxycarbonylaminoacrylimidic acid benzyl ester (282 g, 798 mmol) in acetonitrile (2 L) was added pyridine (129 mL, 1.60 mol). Next was added a solution of bromine (41.1 mL, 798 mmol) in acetonitrile (200 mL) over 15 minutes. The reaction was stirred at 0° C. for an additional 1 hour and then at ambient temperature for 2 hour. The mixture was placed in the refrigerator and held at SIC overnight. The solid product was filtered and washed with 0° C. ether (1 L), dried in the same funnel by drawing air through the solid for 4 hours. The solid was added to water (1 L), stirred vigorously for 1 hour, filtered and dried in the same funnel by drawing air through the solid overnight to afford a white solid (320 g pure though still containing some water) that was used, as is, in the next step. 1H NMR (400 MHz, DMSO) δ 5.35 (s, 2H), 7.25-7.45 (m, 10H), 13.20 (broad s, 1H) ppm; MS (APCI, m/z): 350 [M−H]−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790902B2
Source datasetuspto-grants-2010_09
ORD IDord-86979b543ba745b4b6ac3a077665f46f
Source noteuspto-grants-2010_09