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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1174899Generated: October 27, 2026

Oxalyl chloride → N-[2-(3-Dimethylamino-pyrrolidin-1-yl)-benzothiazol-6-yl]-3-naphthalen-2-yl-acrylamide

https://huagongshe.com/reaction/1174899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant3-(Naphthalen-2-yl)acrylic acidHCID 607737—
Reactant2-(3-Dimethylamino-pyrrolidin-1-yl)-benzothiazol-6-ylamineHCID 63231507—
ProductN-[2-(3-Dimethylamino-pyrrolidin-1-yl)-benzothiazol-6-yl]-3-naphthalen-2-yl-acrylamideHCID 6877457096%

Reaction Steps

Prepare according to Method C (Example 9), using 3-(2-naphthyl)acrylic acid (69 mg, 0.348 mmol), oxalyl chloride (150 μL, 1.72 mmol), and 2-(3-dimethylamino-pyrrolidin-1-yl)-benzothiazol-6-ylamine (60 mg, 0.229 mmol) to afford the title compound (97 mg, 96%). mass spectrum (m/e): 442.0 [M+H]. 1H NMR (400 MHz, DMSO-d6) δ 10.27 (s, 1H), 8.30 (d, 1H, J=1.3 Hz), 8.14 (s, 1H), 8.00-7.92 (m, 3H), 7.78 (dd, 1H, J=8.5, 1.6 Hz), 7.71 (d, 1H, J=15.6), 7.59-7.54 (m, 2H), 7.45-7.42 (m, 2H), 6.97 (d, 1H, J=15.4 Hz), 3.71 (t, 1H, J=8.1 Hz), 3.62 (t, 1H, J=7.9 Hz), 3.47 (m, 1H), 3.26 (m, 1H), 2.89 (m, 1H), 2.21-2.17 (m, 7H), 1.94-1.86 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07838543B2
Source datasetuspto-grants-2010_11
ORD IDord-9d23cc35240c4df8b890a5a6e56a5944
Source noteuspto-grants-2010_11