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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 632648Generated: October 30, 2026

Ammonium Chloride → HCID 86730665, compound

https://huagongshe.com/reaction/632648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 86730666HCID 86730666—
SolventDimethylformamideHCID 6228—
ProductHCID 86730665HCID 8673066585.2%

Reaction Steps

(E)-3-(4-((2-(4-fluorophenyl)-6-methoxybenzo[b]thiophen-3-yl)oxy)phenyl)acrylic acid (48 mg, 0.115 mmol) was dissolved in DMF (3.00 mL). The vial was charged with HATU (65.6 mg, 0.173 mmol), DIEA (0.060 mL, 0.345 mmol), and NH4Cl (6.16 mg, 0.115 mmol). The reaction mixture was stirred for 10 min at room temperature. The reaction was quenched with sat. NH4Cl and diluted with DCM. The organic phase was collected (phase separator) and concentrated by vacuum to afford to crude product. The crude material was purified by reverse phase HPLC (neutral condition, 3% 1-propanol in 1-100% CH3CN/H2O) to afford (E)-3-(4-((2-(4-fluorophenyl)-6-methoxybenzo[b]thiophen-3-yl)oxy)phenyl)acrylamide (41 mg, 0.098 mmol, 85% yield) as a pale orange solid. 1H NMR (400 MHz, CD3OD) δ ppm==3.77 (s, 3 H) 6.40 (d, J=15.66 Hz, 1 H) 6.78-6.90 (m, 3 H) 6.95-7.06 (m, 2 H) 7.16 (d, J=8.59 Hz, 1 H) 7.29-7.49 (m, 4 H) 7.55-7.69 (m, 2 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321746B2
Source datasetuspto-grants-2016_04
ORD IDord-661e22ce79bb4445a91c95deab731c64
Source noteuspto-grants-2016_04