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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377473Generated: November 1, 2026

Sodium borohydride → 3-Hydroxymethyl-8-(2-methoxycarbonylamino-6-methylbenzylamino)-2-methylimidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1377473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 22914804HCID 22914804—
CatalystHydrochloric AcidHCID 313—
SolventMethanolHCID 887—
Product3-Hydroxymethyl-8-(2-methoxycarbonylamino-6-methylbenzylamino)-2-methylimidazo[1,2-a]pyridineHCID 1611831364.6%

Reaction Steps

2 g of 3-formyl-8-(2-methoxycarbonylamino-6-methylbenzylamino)-2-methylimidazo[1,2-a]pyridine are suspended in 30 ml of methanol at RT, 0.2 g of sodium borohydride is added in portions, and the mixture is stirred at RT for 1 h. Subsequently, half the solvent is stripped off in vacuo, the residue is poured into ice-water, and the mixture is neutralized with a few drops of dilute hydrochloric acid and extracted four times with ethyl acetate. The collected organic phases are washed with water and dried over sodium sulfate. The solvent is stripped off in vacuo. The remaining yellowish residue completely crystallizes after some time. Recrystallization from ethyl acetate results in 1.3 g of the title compound of m.p. 170°-172° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665730
Source datasetuspto-grants-1997_09
ORD IDord-91151f26908c425383c869142beda47a
Source noteuspto-grants-1997_09