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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 872794Generated: October 31, 2026

Sodium borohydride → HCID 178466827, compound

https://huagongshe.com/reaction/872794

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 70657267HCID 70657267—
ProductHCID 178466827HCID 178466827—

Reaction Steps

The title compound was prepared from (S)-3-acetyl-N-(1-(3-(3,5-dichloro-4-cyanophenyl)-1H-pyrazol-1-yl)propan-2-yl)-1H-pyrazole-5-carboxamide (63 mg, 0.15 mmol) and sodium borohydride (11 mg, 0.29 mmol) using the method of Example 84. Yield 15 mg. 1H NMR (400 MHz; CDCl3): δ 1.23 (d, 3H), 1.54 (d, 3H), 4.34 (m, 2H), 4.54 (m, 1H), 4.96 (q, 1H), 6.61 (m, 2H), 7.52 (d, 1H), 7.90 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975254B2
Source datasetuspto-grants-2015_03
ORD IDord-5d70d98d367441e499499d84a610f618
Source noteuspto-grants-2015_03