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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 417891Generated: October 30, 2026

Formic Acid → 4-(2-amino-4-chloro-7-((4-methoxy-3,5-dimethylpyridin-2-yl)methyl)-7H-pyrrolo[2,3-d]pyrimidin-5-yl)but-3-ynyl sulfamate

https://huagongshe.com/reaction/417891

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantChlorosulfonyl isocyanateHCID 70918—
Reactant4-[2-Amino-4-chloro-7-(4-methoxy-3,5-dimethyl-pyridin-2-ylmethyl)-7H-pyrrolo[2,3-d]pyrimidin-5-yl]-but-3-yn-1-olHCID 11950510—
CatalystDimethylacetamideHCID 31374—
SolventDichloromethaneHCID 6344—
SolventDimethylacetamideHCID 31374—
Product4-(2-amino-4-chloro-7-((4-methoxy-3,5-dimethylpyridin-2-yl)methyl)-7H-pyrrolo[2,3-d]pyrimidin-5-yl)but-3-ynyl sulfamateHCID 57713864—

Reaction Steps

A mixture of formic acid (0.463 g) and N,N-dimethylacetamide (1 drop) was added to a solution of chlorosulfonyl isocyanate (1.31 g) in DCM (9 mL), and heated to reflux for 3 h. The resulting solution was added to a solution of 4-[2-Amino-4-chloro-7-(4-methoxy-3,5-dimethyl-pyridin-2-ylmethyl)-7H-pyrrolo[2,3-d]pyrimidin-5-yl]-but-3-yn-1-ol (see example 2) (200 mg) in DMA (10 mL) and stirred at rt for 30 min. Work-up and reverse-phase preparative HPLC gave the title compound, as a solid. HPLC Rt=4.96 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093229B2
Source datasetuspto-grants-2012_01
ORD IDord-9e95050e76b04f0b9605a03b584eba05
Source noteuspto-grants-2012_01