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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248976Generated: October 25, 2026

Sodium Hydroxide → 2,4-Diamino-6-(hydroxymethyl)pyrido[2,3-d]pyrimidine

https://huagongshe.com/reaction/1248976

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium borohydrideHCID 4311764—
Reactant2,4-Diaminopyrido[2,3-d]pyrimidine-6-carboxaldehyde hydrochlorideHCID 12908476—
SolventDimethylacetamideHCID 31374—
Product2,4-Diamino-6-(hydroxymethyl)pyrido[2,3-d]pyrimidineHCID 487416—

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 2,4-diaminopyrido[2,3-d]pyrimidine-6-carboxaldehyde hydrochloride (200 mg, 0.884 mmol) in DMAC (40 ml) at 0° C. was treated with 1N NaOH (0.884 ml, 0.884 mmol) followed by a suspension of NaBH4 (16.7 mg, 0.442 mmol) in DMAC (1 ml). The solution was stirred at 25° C. for 30 minutes and evaporated to dryness under high vacuum. A stirred suspension of the residue in H2O (5 ml) was adjusted to pH 3 with 6N HCl, stirred for 5 minutes and adjusted to pH 7 with 1N NaOH. The precipitate was collected by filtration, washed with H2O and dried in vacuo (P2O5); yield 121 mg (51%); mass spectrum, m/e 191 (M)+, 87 (M)+ for DMAC, 36 (M)+ for HCl; λmax nm (εx 10-3): 0.1N HCl-274 (6.91), 318 (8.21), 330 sh (7.17), 362 (1.77); pH 7-248 (18.1), 271 (9.85), 338 (6.52); 0.1N NaOH-248 (19.7), 271 (10.3), 345 (7.14).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04628089
Source datasetuspto-grants-1986_12
ORD IDord-9228b1bc7a0b4358b53b8f339919365e
Source noteuspto-grants-1986_12