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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | HCID 178511143 | HCID 178511143 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Phenyl (3-(benzyloxy)-4-cyanoisothiazol-5-yl)carbamate | HCID 29939179 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07790902B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-86979b543ba745b4b6ac3a077665f46f |
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| Source note | uspto-grants-2010_09 |
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