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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066518Generated: November 3, 2026

Hydrochloric Acid → HCID 178489614, compound

https://huagongshe.com/reaction/1066518

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 54194846HCID 54194846—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178489614HCID 178489614—

Reaction Steps

60 mg of 5-methyl-pyridine-2-sulfonic acid [2-(2-allyloxy-pyridin-4-yl)-6-methoxy-5-(2-methoxy-phenoxy)-pyrimidin-4-yl]-amide, product of example 39, were suspended in THF (5 ml), treated at RT with 2.2 mg of tetrakis-(triphenylphosphine)palladium and stirred for 5 minutes after which time 6.4 mg of NaBH4 were added. The mixture was stirred for 2 h until the reaction was completed according to TLC analysis. The reaction mixture was poured into cold diluted HCl, the product extracted into AcOEt. The organic layer was dried over NaSO4 and the solvent removed in vacuo to give 5-methyl-pyridine-2-sulfonic acid [2-(2-hydroxy-pyridin-4-yl)-6-methoxy-5-(2-methoxy-phenoxy)-pyrimidin-4-yl]-amide as a light yellow solid. ISN mass spectrum, m/e 494.1 (M−1 calculated for C23H21N5O6S: 494).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06242601B1
Source datasetuspto-grants-2001_06
ORD IDord-ce3a518b14f648ffa9f370a2b080024b
Source noteuspto-grants-2001_06