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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298677Generated: October 27, 2026

5-Indanecarboxaldehyde → Methyl 4-(indan-5-ylamino)-5-methylthiothiophene-2-carboxylate

https://huagongshe.com/reaction/2298677

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-IndanecarboxaldehydeHCID 121624—
ReactantMethyl 4-amino-5-methylthiothiophene-2-carboxylateHCID 86583856—
ProductMethyl 4-(indan-5-ylamino)-5-methylthiothiophene-2-carboxylateHCID 86758690—

Reaction Steps

Using the procedure described in Example 220, step (a), 60 mg (0.29 mmol) of methyl 4-amino-5-methylthiothiophene-2-carboxylate, 42.3 mg (0.29 mmol) of 5-indancarboxaldehyde, and 135 mg (2.2 equiv, 0.63 mmol) of NaHB(OAc)3 were allowed to react to give methyl 4-(indan-5-ylamino)-5-methylthiothiophene-2-carboxylate. Mass spectrum (ESI, m/z): Calcd. for C17H19NO2S2, 334.09 (M+H), found 332.3 (imine), 333.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492403B1
Source datasetuspto-grants-2002_12
ORD IDord-f060671ec0bf4771b6f9648f2327acd0
Source noteuspto-grants-2002_12