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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588156Generated: October 25, 2026

Methylcarbamoyl chloride → (6-chloro-3-methoxy-1-trityl-1H-pyrazolo[4,3-c]pyridin-4-yl)methyl methylcarbamate

https://huagongshe.com/reaction/588156

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylcarbamoyl chlorideHCID 80931—
ReactantDiisopropylethylamineHCID 81531—
Reactant(6-chloro-3-methoxy-1-trityl-1H-pyrazolo[4,3-c]pyridin-4-yl)methanolHCID 118271763—
SolventDichloromethaneHCID 6344—
Product(6-chloro-3-methoxy-1-trityl-1H-pyrazolo[4,3-c]pyridin-4-yl)methyl methylcarbamateHCID 11827230476.3%

Reaction Conditions

Temperature35 °C

Reaction Steps

A solution of (6-chloro-3-methoxy-1-trityl-1H-pyrazolo[4,3-c]pyridin-4-yl)methanol (Intermediate 35B, 200 mg, 0.439 mmol) and methylaminoformyl chloride (45.1 mg, 0.483 mmol) in DCM (1462 μl) was treated with DIEA (153 μl, 0.877 mmol) and stirred @ 35° C. for 1 h Reaction was dilluted in with DCM and concentrated in vacuo on silica. Material was purified by normal phase column chromotography eluting with Hex/EtOAc (0-40%) affording (6-chloro-3-methoxy-1-trityl-1H-pyrazolo[4,3-c]pyridin-4-yl)methyl methylcarbamate (172 mg, 0.335 mmol, 76% yield) as a white solid. MS: [M+H]+ m/z 513.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09226922B2
Source datasetuspto-grants-2016_01
ORD IDord-7e22731b8e114406993c3d8de19fee65
Source noteuspto-grants-2016_01