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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2089313Generated: October 30, 2026

5-Chloro-1-(cyclopropylmethyl)-4-nitro-1h-pyrazole → (R)-N-(1-(1-cyclopropylmethyl-4-nitro-1H-pyrazol-5-yl)azepan-4-yl)-2,2,2-trifluoroacetamide

https://huagongshe.com/reaction/2089313

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloro-1-(cyclopropylmethyl)-4-nitro-1h-pyrazoleHCID 58464813—
Reactant(R)-N-(azepan-4-yl)-2,2,2-trifluoroacetamideHCID 86658411—
Product(R)-N-(1-(1-cyclopropylmethyl-4-nitro-1H-pyrazol-5-yl)azepan-4-yl)-2,2,2-trifluoroacetamideHCID 8665841455%

Reaction Steps

Following the procedure for Example 503 starting with 5-chloro-1-cyclopropylmethyl-4-nitro-1H-pyrazole and (R)-2,2,2-trifluoro-N-(hexahydro-1H-azepin-4-yl)-acetamide gave (R)-N-(1-(1-cyclopropylmethyl-4-nitro-1H-pyrazol-5-yl)azepan-4-yl)-2,2,2-trifluoroacetamide as a pale yellow gum (0.98 g, 55%). 1H-NMR (400 MHz, CDCl3) δ 8.08 (s, 1H), 6.42-6.39 (m, 1H), 4.22-4.14 (m, 1H), 4.00-3.85 (m, 2H), 3.44-3.32 (m, 1H), 3.30-3.15 (m, 3H), 2.25-2.05 (m, 2H), 2.00-1.75 (m, 4H), 1.30-1.20 (m, 1H), 0.70-0.62 (m, 2H), 0.50-0.35 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436001B2
Source datasetuspto-grants-2013_05
ORD IDord-29bc7de92fd744a8ada68e98437325c6
Source noteuspto-grants-2013_05