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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1924840Generated: October 30, 2026

2,3-dihydro-1H-indene-1-carboxamide → Indanyl 1,3-oxazolidine

https://huagongshe.com/reaction/1924840

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-dihydro-1H-indene-1-carboxamideHCID 118099—
Reactant[(2-Chloroethyl)amino]-n-(4-fluoroindanyl)carboxamideHCID 59355772—
ProductIndanyl 1,3-oxazolidineHCID 67522069—

Reaction Steps

As depicted in Scheme 2, the reaction of an appropriately substituted indanyl amine, for example 4-fluoroindanylamine (known compound, U.S. Pat. No. 5,486,541) with 2-chloroethyl isocyanate (SM4) under basic conditions, in an appropriate solvent yielded the corresponding indanyl carboxamide intermediate (a), for example, [(2-chloroethyl)amino]-N-(4-fluoroindanyl)carboxamide. Intermediate (a) was heated under basic conditions in an appropriate solvent to yield the appropriate indanyl 1,3-oxazolidine, a compound of formula I and an intermediate (b), for example, 2-[aza(4-fluoroindanyl)methylene]-1,3-oxazolidine, described in detail in Example 2, Step B, as set forth below. Compound (b) was reacted with an isothiocyanate, for example, methyl isothiocyanate, under basic conditions yielding the corresponding amino methane-1-thione, for example, 2-[aza(4-fluoroindanyl)methylene](1,3-oxazolidin-3-yl)(methylamino)methane-1-thione, a compound of formula I, described in detail in Example 2, Step C, as set forth below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178567B2
Source datasetuspto-grants-2012_05
ORD IDord-cc3a70a4eee044dd8712f85061dd6a1c
Source noteuspto-grants-2012_05