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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2417922Generated: November 3, 2026

Acetic Anhydride → HCID 13338631, compound

https://huagongshe.com/reaction/2417922

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant3,4-Dihydro-2H-pyrimido[2,1-b][1,3]benzothiazol-7-amineHCID 13338584—
ProductHCID 13338631HCID 13338631—

Reaction Steps

To 25 parts of acetic acid anhydride are added portionwise 1.3 parts of 3,4-dihydro-2H-pyrimido[2,1-b]benzothiazol-7-amine (exothermic reaction: temp. rises to 30° C.). Upon completion, stirring is continued for one hour at room temperature. After cooling to 5°-10° C., the precipitated product is filtered off and dissolved in water. The solution is treated with activated charcoal. The latter is filtered off over hyflo and the filtrate is alkalized with a few drops of ammonium hydroxide. Upon stirring, the product is allowed to crystallize. It is filtered off and dried, yielding 0.8 parts of N-(3,4-dihydro-2H-pyrimido[2,1-b]benzothiazol-7-yl)acetamide; mp. 178° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04471117
Source datasetuspto-grants-1984_09
ORD IDord-6c79ee46d34c4fef968c8a99cf03eb6d
Source noteuspto-grants-1984_09