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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412985Generated: October 28, 2026

Ammonium Chloride → HCID 18537269, compound

https://huagongshe.com/reaction/412985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantTrimethylaluminumHCID 16682925—
ReactantHCID 18537031HCID 18537031—
ReactantHCID 18537479HCID 18537479—
SolventTolueneHCID 1140—
ProductHCID 18537269HCID 18537269—

Reaction Steps

5-Methylthio-4-(phenylsulfonyl)thiophene-2-carboxamidine trifluoroacetate: The same procedure as in Example 257, step (b) was followed using 13.8 mg (0.044 mmol) of methyl 5-methylthio-4-(phenylsulfonyl)thiophene-2-carboxylate (as prepared in the step before), 20 mg of ammonium chloride (0.376 mmol), 0.176 ml of trimethylaluminum (2.0 M in toluene, 0.353 mmol) and 3 ml of anhydrous toluene and chromatographed as before by preparative reverse phase HPLC performed with a Rainin SD-1 Dynamax system and a 2-in. C18 reverse phase Dynamax 60A column using a gradient of 30% MeOH /0.1% TFA in water to 100% MeOH and a flow rate of 50 mL/ min to yield 2.3 mg of 5-methylthio-4-(phenylsulfonyl)thiophene-2-carboxamidine. 1H-NMR (CD3OD, 400 MHz) δ 8.42 (s, 1H), 8.04 (m, 2H), 7.70 (m, 2H), 7.62 (m, 1H) and 2.70 (s, 3H). Mass spectrum (ESI, m/z): Calcd. C12Hi2N2O2S3, 313.0 (M+H), found 313.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06562840B1
Source datasetuspto-grants-2003_05
ORD IDord-760a58c7d2f74fc58cd769b6cea507d1
Source noteuspto-grants-2003_05