HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Indanecarboxaldehyde → Methyl 4-(indan-5-ylamino)-5-methylthiothiophene-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Indanecarboxaldehyde | HCID 121624 | — |
| Reactant | Methyl 4-amino-5-methylthiothiophene-2-carboxylate | HCID 86583856 | — |
| Product | Methyl 4-(indan-5-ylamino)-5-methylthiothiophene-2-carboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06492403B1 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-f060671ec0bf4771b6f9648f2327acd0 |
| Source note | uspto-grants-2002_12 |