HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1909948Generated: October 31, 2026
2-Naphthaleneacetic acid → HCID 53469633, compound
https://huagongshe.com/reaction/1909948
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Naphthaleneacetic acid | HCID 11393 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | 3-(2,3-dihydro-1H-indol-5-yl)thieno[3,2-c]pyridin-4-amine | HCID 66823569 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 53469633 | HCID 53469633 | 43% |
Reaction Steps
To a 4 mL screw cap vial was added 3-(2,3-dihydro-1H-indol-5-yl)thieno[3,2-c]pyridin-4-amine (100 mg, 0.374 mmol) followed by HATU (142 mg, 0.374 mmol), 2-napthylacetic acid (69.6 mg, 0.374 mmol) and DIEA (0.261 mL, 1.496 mmol). N,N-Dimethylformamide (DMF) (2 mL) was added and the reaction was sealed and left to stir at room temperature overnight. The reaction mixture was poured into water (4 mL) and extracted with EtOAc (5 mL). The organics were dried over Na2SO4 and concentrated. The residue was taken up in DCM and purified via normal phase chromatography (0-10% MeOH/DCM). Fractions were collected and concentrated to afford 3-[1-(2-naphthalenylacetyl)-2,3-dihydro-1H-indol-5-yl]thieno[3,2-c]pyridin-4-amine (70 mg). LC/MS (ES) m/z=436.2 [M+H]+ 1H NMR (400 MHz, DMSO-d6) δ ppm 3.19-3.29 (m, 2H) 4.07 (s, 2H) 4.31 (t, J=8.46 Hz, 2H) 5.45 (br. s., 2H) 7.20-7.29 (m, 2H) 7.33 (s, 1H) 7.42 (s, 1H) 7.46-7.55 (m, 3H) 7.80-7.85 (m, 2H) 7.86-7.95 (m, 3H) 8.18 (d, J=8.08 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08598156B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-11c040ab26f647d180f80ecc66e5ee0a |
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| Source note | uspto-grants-2013_12 |
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