HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243274Generated: October 29, 2026
Diisopropylethylamine → HCID 178463589, compound
https://huagongshe.com/reaction/243274
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-(3-Phenylbenzo[b]thiophen-2-yl)ethanamine | HCID 58459144 | — |
| Reactant | HCID 178478393 | HCID 178478393 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 178463589 | HCID 178463589 | — |
Reaction Steps
A mixture of 1-(3-phenylbenzo[b]thiophen-2-yl)ethylamine from Example 23 (160 mg, 0.63 mmol), 6-chloro-9H-purine (98 mg, 0.63 mmol) and DIPEA (0.16 mL, 0.95 mmol) in n-butanol (1.3 mL) was stirred in a sealed vial for 3 days at 120° C. After cooling to RT, the crude reaction mixture was loaded into an Isolute® SCX-2 which was washed with MeOH and the product eluted with 2M NH3/MeOH. The product containing fractions were combined and concentrated in vacuo and the resulting residue was purified by column chromatography (Si—PCC, gradient 0-6% MeOH in DCM) and then triturated with EtOAc affording 101 (105 mg, 45%). LCMS: RT 4.33 min [M+H]+ 372.1. 1H NMR (DMSO, 400 MHz): δ 8.21 (1H, s), 8.16-8.10 (2H, m), 7.92-7.86 (1H, m), 7.66-7.54 (4H, m), 7.50-7.44 (1H, m), 7.37-7.26 (3H, m), 5.76 (1H, s), 1.50 (3H, d, J=6.94 Hz)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08653089B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-8e5bfa5e8a124faf8ed032c7dbc67e1d |
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| Source note | uspto-grants-2014_02 |
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