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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 80655Generated: October 26, 2026

Cyclopropanesulfonyl chloride → 5-((2-(1-(Cyclopropylsulfonyl)piperidin-4-yl)-2H-1,2,3-triazol-4-yl)methoxy)-2-(1H-tetrazol-1-yl)pyridine

https://huagongshe.com/reaction/80655

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropanesulfonyl chlorideHCID 2760919—
Reactant5-((2-(piperidin-4-yl)-2H-1,2,3-triazol-4-yl)methoxy)-2-(1H-tetrazol-1-yl)pyridine hydrochlorideHCID 68746624—
Product5-((2-(1-(Cyclopropylsulfonyl)piperidin-4-yl)-2H-1,2,3-triazol-4-yl)methoxy)-2-(1H-tetrazol-1-yl)pyridineHCID 25174271—

Reaction Steps

The title compound was synthesized using Intermediate 15 and cyclopropanesulfonyl chloride in a similar manner as described in Example 39. 1H NMR (DMSO-d6): δ 9.45 (1H, s), 8.28 (1H, d), 8.03 (1H, d), 7.73 (1H, s), 7.58 (1H, dd), 5.28 (2H, s), 4.62 (1H, m), 3.87 (2H, m), 3.12 (2H, m) 2.31 (5H, m), 1.86 (2H, m), 1.02 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846675B2
Source datasetuspto-grants-2014_09
ORD IDord-217521ea7aa848df83f85fc6cce8dfc6
Source noteuspto-grants-2014_09