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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809057Generated: November 1, 2026

Azepane → HCID 42644590, compound

https://huagongshe.com/reaction/1809057

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzepaneHCID 8119—
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 59542554HCID 59542554—
SolventDimethylformamideHCID 6228—
ProductHCID 42644590HCID 4264459027.8%

Reaction Steps

4-(4-Carboxy-thiophen-2-yl)-piperidine-1-carboxylic acid benzyl ester (0.095 g, 0.27 mmol) was dissolved in DMF (2 mL). DIPEA (0.54 mmol), HATU (0.27 mmol) and homopiperidine (0.27 mmol) were added and the reaction stirred at room temperature for 1 hour. The reaction mixture was partitioned between ethyl acetate and water. The organic solution was separated and dried with magnesium sulphate, filtered and the solvent removed under vacuum. The residue was purified by HPLC, eluting with 40%-90% acetonitrile in water (0.1% formic acid) over 30 minutes. The fractions containing the desired product were concentrated under vacuum to give the title compound (0.032 g). LCMS m/z 427.29 [M+H]+ RT=12.22 min (Analytical Method 1). 1H NMR (400 MHz, CHCl3-d): δ 7.4-7.35 (m, 4H), 7.35-7.3 (m, 1H), 7.25 (s, 1H), 6.9 (s, 1H), 5.15 (s, 2H), 4.3 (m, 2H), 3.6 (m, 2H), 3.5 (m, 2H), 3.00-2.90 (m, 3H), 2.0 (m, 2H), 1.8 (m, 2H), 1.75-1.5 (m, 8H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362008B2
Source datasetuspto-grants-2013_01
ORD IDord-a2fea5a6315642e99e59e21d351dd597
Source noteuspto-grants-2013_01