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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791328Generated: November 3, 2026

Sodium borohydride → methyl 4-amino-1H-indazole-1-carboxylate

https://huagongshe.com/reaction/1791328

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactantmethyl 4-nitro-1H-indazole-1-carboxylateHCID 22032604—
SolventEthanolHCID 702—
Productmethyl 4-amino-1H-indazole-1-carboxylateHCID 2203265283.7%

Reaction Steps

The product of Example 90A (1.66 g, 7.5 mmol) in ethanol (20 mL) was treated with BiCl3 (8.2 g, 2.6 mmol) followed by the addition of NaBH4 (1.13 g, 30.5 mmol). The reaction mixture was stirred at room temperature for 20 minutes, filtered through Celite, and the filtrate was evaporated under reduced pressure. The residue was partitioned between ethyl acetate/dilute NaHCO3 solution. The organic phase was separated, dried over MgSO4, filtered and the filtrate concentrated under reduced pressure to provide the title compound (1.2 g). 1H NMR (300 MHz, DMSO-d6) δ 6.1 (s, 2H), 6.41 (dd, 1H), 7.21 (m, 2H), 8.42 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074805B2
Source datasetuspto-grants-2006_07
ORD IDord-76f351b7aaeb48c2a08b8b641d36c13e
Source noteuspto-grants-2006_07