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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972764Generated: November 1, 2026

Formaldehyde → HCID 58529713, compound

https://huagongshe.com/reaction/1972764

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 16066662HCID 16066662—
SolventDichloromethaneHCID 6344—
ProductHCID 58529713HCID 5852971317%

Reaction Steps

To a solution of 5-(2-benzyl-2H-indazol-6-yl)-7-piperidin-4-ylpyrrolo[2,1-f][1,2,4]triazin-4-amine (75 mg, 0.18 mmol) in dichloromethane (2 mL) was added formaldehyde (37% solution in water) (80 μL, 1.06 mmol) and sodium triacetoxyborohydride (113 mg, 0.53 mmol). The reaction was stirred (rt) for 17 h. The mixture was diluted with dichloromethane and was washed with H2O (1×10 mL). The organic phase was washed with brine, and was dried (Na2SO4) and concentrated. The residue was purified by preparative HPLC using a gradient elution from 15% to 50% acetonitrile in water to obtain 13 mg (17%) of the desired product. 1H NMR (300 MHz, DMSO-d6) δ 8.54 (s, 1 H), 7.88 (s, 1 H), 7.79 (d, 1 H), 7.58 (s, 1 H), 7.37-7.28 (m, 5 H), 7.14 (dd, 1 H), 6.58 (s, 1 H), 5.65 (s, 2 H), 3.11-2.97 (m, 1 H), 2.85 (d, 2 H), 2.18 (s, 3 H), 2.04-1.94 (m, 4H), 1.77-1.61 (m, 2 H); ES-MS m/z 438.3 [M+H]+, HPLC RT (min) 2.11.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431695B2
Source datasetuspto-grants-2013_04
ORD IDord-42120bd0e2024e808bfbc8f510ed069c
Source noteuspto-grants-2013_04