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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595491Generated: October 29, 2026

Acetic Anhydride → HCID 89689617, compound

https://huagongshe.com/reaction/595491

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium hydrideHCID 24758—
ReactantHCID 89689645HCID 89689645—
SolventTetrahydrofuranHCID 8028—
ProductHCID 89689617HCID 89689617—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of tert-butyl 2-(6-(benzo[d]thiazol-6-ylamino)-4-(isopropylamino)pyridin-3-yl)-5-methyloxazol-4-ylcarbamate (Example 106) (20 mg, 0.042 mmol) in Tetrahydrofuran (5 mL) was cooled to 0° C. and treated with NaH (0.042 mmol). Stirred the reaction mixture at 0° C. for 10 min. Added Ac2O (0.042 mmol) to the reaction mixture and stirred at 0° C. for 0.5 h. The reaction mixture was quenched with ice pieces and extracted with ethyl acetate. The organic layer was separated, dried over Na2SO4, filtered and concentrated to afford tert-butyl acetyl(2-(6-(benzo[d]thiazol-6-ylamino)-4-(isopropylamino)pyridin-3-yl)-5-methyloxazol-4-yl)carbamate. LC/MS: Acquity BEH C18 2.1×50 mm, 1.8 micron; Solvent A=0.1% TFA in water; Solvent B=0.1% TFA in ACN; gradient 0-100% B over 2 min; retention time: 0.90 min; LCMS (ES-API), m/z 523.6 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242976B2
Source datasetuspto-grants-2016_01
ORD IDord-2aa07eed689a440e839a8440c5af4752
Source noteuspto-grants-2016_01