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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2214205Generated: November 1, 2026

Formaldehyde → HCID 10207696, compound

https://huagongshe.com/reaction/2214205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 10300352HCID 10300352—
SolventEthanolHCID 702—
ProductHCID 10207696HCID 10207696—

Reaction Steps

N-[3,3-Dimethyl-1-(4-piperidylmethyl)indolin-6-yl][2-(1H-indazol-6-ylamino)(3-pyridyl)]carboxamide (140 mg, Example 41) was dissolved in 10 mL EtOH. Formaldehyde (10 mL, 37%) was added, followed by 100 mg of NaCNBH3. The mixture was stirred at RT overnight, and concentrated in vacuo. The crude was extracted between saturated NaHCO3 solution and EtOAc, the resulting organic layer was dried over MgSO4, filtered and concentrated in vacuo to afford a yellow solid. This material was further purified by preparative HPLC to yield a white solid. MS: 510 (M+1). Calc'd. for C30H35N7O—509.6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105682B2
Source datasetuspto-grants-2006_09
ORD IDord-26d516658a8a45abb738bea97470cbc7
Source noteuspto-grants-2006_09