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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1840341Generated: October 30, 2026

Cyanamide → HCID 178486145, compound

https://huagongshe.com/reaction/1840341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanamideHCID 9864—
ReactantCesium fluorideHCID 25953—
ReactantDiisopropylethylamineHCID 81531—
ReactantN-[4-Chloro-2-tert-butyldimethylsilyloxy-3-(N'',N''-dimethylaninosulfonyl)phenyl]-N'-(2-bromophenyl)carbodiimideHCID 23447747—
SolventAcetonitrileHCID 6342—
ProductHCID 178486145HCID 17848614530.2%

Reaction Steps

To a solution of N-[4-chloro-2-tert-butyldimethylsilyloxy-3-(N″,N″-dimethylaminosulfonyl)phenyl]-N′-(2-bromophenyl)carbodiimide (266 mg, 0.49 mmol) in acetonitrile (5 mL) at room temperature, cyanamide (83 mg, 1.96 mmol) and N,N-diisopropylethylamine (76 mg, 0.59 mmol) was added. The reaction mixture was stirred at room temperature for 1 hour. The reaction mixture was concentrated under reduced pressure. The residue was diluted with a mixture of THF (3 mL) and methanol (1 mL). Cesium fluoride (90 mg, 0.59 mmol) was added at 0° C. The reaction mixture was stirred at 0° C. for 3 hours. The reaction mixture was concentrated under reduced pressure. The residue was purified by Gilson HPLC to give the desired product (70 mg, 30%). EI-MS m/z 473.75(M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06680317B2
Source datasetuspto-grants-2004_01
ORD IDord-05875caedfc64b1faad04da37088892e
Source noteuspto-grants-2004_01