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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2053004Generated: November 1, 2026

Acetic Anhydride → HCID 178474854, compound

https://huagongshe.com/reaction/2053004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 178511295HCID 178511295—
SolventDimethylformamideHCID 6228—
ProductHCID 178474854HCID 178474854—

Reaction Steps

To a solution of 50 mg (0.125 mmol) of trans-7-(3-aminomethyl-cyclobutyl)-5-(3-benzyloxy-phenyl)-7H-pyrrolo[2,3-d]pyrimidin-4-ylamine in 2 ml of anhydrous N,N-dimethylformamide is added 13 μl (0.138 mmol) of acetic anhydride (Fluka, Buchs, Switzerland). After stirring 1 h at RT, working-up is effected by partitioning between water and ethyl acetate. The organic layer is dried over magnesium sulfate and evaporated to dryness to provide trans-N-{3-[4-amino-5-(3-benzyloxy-phenyl)-pyrrolo[2,3-d]pyrimidin-7-yl]-cyclobutylmethyl}-acetamide. Analytical HPLC: tR=6.65 min (Grad 2); ES-MS: m/eo=442.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07326699B2
Source datasetuspto-grants-2008_02
ORD IDord-746b02ec570440ccabdf640e03a76403
Source noteuspto-grants-2008_02