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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058463Generated: October 31, 2026

Ammonium Chloride → HCID 69939571, compound

https://huagongshe.com/reaction/1058463

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantTrimethylaluminumHCID 16682925—
ReactantHCID 18536895HCID 18536895—
ReactantHCID 18537238HCID 18537238—
SolventTolueneHCID 1140—
ProductHCID 69939571HCID 6993957182%

Reaction Steps

5-Methylthio-4-(4-phenyl(1,3-oxazol-2-yl))thiophene-2-carboxamidine hydrochloride: Methyl 5-methylthio-4-(4-phenyl(1,3-oxazol-2-yl))thiophene-2-carboxylate (80.3 mg, 0.242 mmol, as prepared in the previous step) was treated according to the procedure in Example 10, step (b) using 155 mg (2.90 mmol) of ammonium chloride in 1.45 mL of toluene and 1.45 mL (2.90 mmol) of 2 M trimethylaluminum in toluene. The resulting light yellow solid was chromatographed on a 5 g silica SPE column (Waters Sep-Pak) with 10% MeOH—CH2Cl2 to give a light yellow resin. Crystallization from MeOH—Et2O (ca. 1:3) afforded the title compound as a yellow solid (62.2 mg, 82%). 1H-NMR (300 MHz, DMSO-d6) δ 9.39 (broad s, 2H), 8.97 (broad s, 2H), 8.78 (s, 1H), 8.60 (s, 1H), 7.89 (d, 2H, J=7 Hz), 7.49 (t, 2H, J=7 Hz), 7.38 (t, 1H, J=7 Hz), and 2.80 (s, 3H). Mass spectrum (ESI) calcd. for C15H13N3OS2: 316.1(M+H). Found: 316.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06515002B2
Source datasetuspto-grants-2003_02
ORD IDord-21b17503551d4b43a7b6acb08761d29b
Source noteuspto-grants-2003_02