HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641895Generated: November 1, 2026
N,O-bis(trimethylsilyl)acetamide → HCID 178418823, compound
https://huagongshe.com/reaction/1641895
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,O-bis(trimethylsilyl)acetamide | HCID 6913588 | — |
| Reactant | HCID 178499113 | HCID 178499113 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 178418823 | HCID 178418823 | — |
Reaction Steps
6-(2,2-Diphenyl-ethylamino)-9H-purine-2-carboxylic acid methyl ester hydrochloride (which is prepared using the method described in international patent application WO 01/94368)(18.2 g, 40.9 mmol) is placed in an oven-dried flask under an atmosphere of argon. Dry CHCl3 (250 mL) and N,O-bis(trimethylsilyl)acetamide (50 mL) are added to the reaction mixture. The reaction mixture is refluxed for 1 hour. The reaction mixture is allowed to cool and the solvent is removed in vacuo. The resulting solid is taken up in MeOH (200 mL) and filtered the white solid is washed with MeOH (2×200 mL). The solid is suspended in water and sonicated for 30 minutes, filtered, washed with water (100 mL), MeOH (2×100 mL) and dried in vac oven to give the title compound. 1H NMR (DMSO, 400 MHz); 8.30 (m, 1H), 8.50 (m, 1H) 7.45-7.20 (m, 10H), 4.80-4.55 (m, 2H), 4.20 (m, 2H), 4.00 (m, 2H), 3.4 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08114877B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-8cc3f313b37f43f6bcad11e195e48e27 |
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| Source note | uspto-grants-2012_02 |
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