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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600659Generated: October 29, 2026

Acetic Acid → HCID 57560985, compound

https://huagongshe.com/reaction/600659

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant2-Cyclopropyl-2-hydroxyacetonitrileHCID 11389359—
ReactantHCID 67273084HCID 67273084—
SolventWaterHCID 962—
ProductHCID 57560985HCID 5756098550%

Reaction Steps

To the suspension of N-(2-azabicyclo[2.2.1]hept-5-yl)-1H-indazole-3-carboxamide hydrochloride (0.36 mmol), cyclopropylcarboxaldehyde (0.9 mmol), and N,N-diisopropylethylamine (1.08 mmol), acetic acid (0.43 mmol) was added sodium triacetoxyborohydride (0.61 mmol). The reaction mixture was maintained at rt for 2 h and was poured into water, extracted with 95/5 dichloromethane/methanol (2×30 mL), and the combined extracts were concentrated. The residue was purified by preparative HPLC, thus providing the product in 50% yield. 1H NMR (CD3OD) δ 8.21 (m, 1H), 7.59 (m, 1H), 7.45 (m, 1H), 7.26 (m, 1H), 4.15 (m, 1H), 3.83 (m, 1H), 3.10 (m, 3H), 2.02 (m, 4H), 1.37 (m, 2H), 0.74 (m, 2H), 0.48 (m, 2H); LC/MS (EI) tR 2.72 min, m/z 311 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902217B2
Source datasetuspto-grants-2011_03
ORD IDord-3cb8a5a2ffb14903856bf828ee5cee20
Source noteuspto-grants-2011_03