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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1190841Generated: October 30, 2026

HCID 68323240, compound → HCID 70800909, compound

https://huagongshe.com/reaction/1190841

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68323240HCID 68323240—
ReactantHCID 178482962HCID 178482962—
SolventDichloromethaneHCID 6344—
ProductHCID 70800909HCID 7080090995%

Reaction Steps

To a solution of (5-((6-phenylbenzo[d]thiazol-2-yl)methyl)-1,3,4-oxadiazol-2-yl)methanamine (788 mg, 2.44 mmol) (described in WO 2011/074560) in DCM (10 mL) was added N-(tert-butoxycarbonyl)-N-[4-(dimethylazaniumylidene)-1,4-dihydropyridin-1-ylsulfonyl]azanide (737 mg, 2.44 mmol) (Winum, J.-Y. et al., Org. Lett., 3(14):2241-2243 (2001)) and the reaction mixture stirred at rt for 3 days. The mixture was diluted with satd. NH4Cl and extracted with EtOAc (3×). The combined extracts were washed with brine, dried (Na2SO4) filtered and concentrated under reduced pressure. The residue was purified by silica gel chromatography eluting with 10-100% EtOAc/DCM to give Compound 46a (1.16 g, 95% yield) as a brown oil. LCMS=0.99 min using analytical method (M), 502.0 (M+H). 1H NMR (400 MHz, CDCl3) δ 8.07 (d, J=8.5 Hz, 1H), 8.06 (s, 1H), 7.74 (dd, J=8.4, 1.9 Hz, 1H), 7.68-7.61 (m, 2H), 7.49 (t, J=7.4 Hz, 2H), 7.44-7.36 (m, 1H), 6.96 (br. s., 1H), 5.26 (br. s., 2H), 4.79 (s, 2H), 4.63 (s, 2H), 1.37 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680090B2
Source datasetuspto-grants-2014_03
ORD IDord-d6ae4b62c19d48e0a98386704f4aee79
Source noteuspto-grants-2014_03