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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2215573Generated: October 31, 2026

Acetic Acid → HCID 21054829, compound

https://huagongshe.com/reaction/2215573

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantFormaldehydeHCID 712—
ReactantSodium hydrido[tris(methanolato)]borate(1-)HCID 3084262—
ReactantHCID 21054831HCID 21054831—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21054829HCID 2105482967.1%

Reaction Steps

5-(2-(3-Ethylureido)pyridin-4-yloxy)indole-1-carboxylic acid piperidin-4-ylamide (36 mg, 0.085 mmol, Example 181) was dissolved in tetrahydrofuran (2.0 ml) and methanol (1.0 ml); and a 37% aqueous formaldehyde solution (0.036 ml, 0.43 mmol) and acetic acid (0.0098 ml, 0.17 mmol) were added thereto. While stirring at room temperature, sodium trimethoxyborohydride (27 mg, 0.13 mmol) was added; and the reaction mixture was stirred for 30 minutes. The reaction mixture was partitioned between ethyl acetate and a saturated aqueous solution of sodium hydrogencarbonate; and the organic layer was washed with brine and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure; the obtained crystals were suspended in diethyl ether, filtered off, washed with diethyl ether, and dried to yield the title compound (25 mg, 0.057 mmol, 67%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109219B2
Source datasetuspto-grants-2006_09
ORD IDord-b14e34248a9e4954bdbde148ab0bd906
Source noteuspto-grants-2006_09