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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390070Generated: October 29, 2026

Dichloromethane → HCID 66553591, compound

https://huagongshe.com/reaction/390070

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantHydrazinium chlorideHCID 115031—
ReactantHCID 86651324HCID 86651324—
CatalystPalladiumHCID 23938—
SolventAmmoniaHCID 222—
ProductHCID 66553591HCID 6655359163%

Reaction Steps

To a suspension of 2-((5-(benzyloxymethyl)-4-chloro-5H-pyrrolo[3,2-d]pyrimidin-7-yl)methylamino)-2-(methylthiomethyl)propane-1,3-diol (9.0 mg, 0.037 mmol) and palladium-black (10 mg) in 7 M methanolic ammonia (2 mL) was added hydrazine hydrochloride (0.250 mL, 6.87 mmol) dropwise. After 1 h at ambient temperature the reaction was virtually complete by TLC (dichloromethane:7 M methanolic ammonia, 3:1, visualised with UV and Erlichs). The supernatant solution was filtered through a small pad of celite and the palladium was washed twice with methanol and also filtered through celite. The combined filtrates were concentrated under reduced pressure and the resulting residue triturated with chloroform and dichloromethane. Lyophilization of the residue gave 2-((4-amino-5H-pyrrolo[3,2-d]pyrimidin-7-yl)methylamino)-2-(methylthiomethyl)propane-1,3-diol (4 mg, 63%) as a white solid. 1H NMR (D2O) δ 8.16 (s, 1H), 7.58 (s, 1H), 4.12 (s, 2H), 3.79-3.70 (m, 4H), 2.85 (s, 2H), 2.15 (s, 3H). +ESMS Found 298.1346 (M+H+) C12H20N5O2S requires 298.1338.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383636B2
Source datasetuspto-grants-2013_02
ORD IDord-0a710ee87cc34635a7f4fe47cf44d218
Source noteuspto-grants-2013_02