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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1840368Generated: November 1, 2026

Cyanamide → HCID 178486148, compound

https://huagongshe.com/reaction/1840368

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanamideHCID 9864—
ReactantCesium fluorideHCID 25953—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 23447819HCID 23447819—
ReactantHCID 178418324HCID 178418324—
ProductHCID 178486148HCID 17848614840%

Reaction Steps

Following the general procedure for cyanoguanidine formation outlined in example 12, N-[4-chloro-2-tert-butyldimethylsilyloxy-3-(N″,N″-dimethylaminosulfonyl)phenyl]-N′-(2-fluorophenyl)carbodiimide (350 mg, 0.72 mmol), cyanamide (121 mg, 2.88 mmol) and N,N-diisopropylethylamine (111 mg, 0.86 mmol) were reacted, followed by desilylation with Cesium fluoride (132 mg, 0.86 mmol) to form the desired product (120 mg, 40%). EI-MS m/z 412.2 (M+). 1H NMR (DMSO-d6) δ 2.86 (s, 6H), 7.20 (m, 2H), 7.27 (m, 2H), 7.40 (t, 1H), 7.52 (d, 1H), 9.06 (s, 1H), 9.20 (s, 1H), 10.51 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06680317B2
Source datasetuspto-grants-2004_01
ORD IDord-2f43855568e94d89840e1355de363fb7
Source noteuspto-grants-2004_01