HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2355841Generated: October 30, 2026
1,1,3,3-Tetramethylguanidine → HCID 68466355, compound
https://huagongshe.com/reaction/2355841
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,1,3,3-Tetramethylguanidine | HCID 66460 | — |
| Reactant | Methyl 2-{[(benzyloxy)carbonyl]amino}-2-(dimethyl phosphono)acetate | HCID 2734718 | — |
| Reactant | tert-Butyl 5-formyl-1H-indazole-1-carboxylate | HCID 22831863 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68466355 | HCID 68466355 | 85% |
Reaction Steps
A solution of N-(benzyloxycarbonyl)-α-phosphonoglycine trimethyl ester (5.50 g, 16.6 mmol) and tetramethylguanidine (1.99 mL, 15.9 mmol) in anhydrous tetrahydrofuran (50 mL) was stirred at −78° C. for 20 min. To this was added a solution of 5-formyl-indazole-1-carboxylic acid tert-butyl ester (3.72 g, 15.1 mmol) in tetrahydrofuran (25 mL) slowly via syringe over 10 min. The reaction mixture was stirred at −78° C. for 4 h and then allowed to warm to room temperature overnight. The solvent was evaporated and the resulting residue subjected to flash column chromatography on silica gel (1:2 ethyl acetate/hexane) giving the title compound as a white foam (5.77 g, 85%). 1H-NMR (CDCl3, 500 MHz) δ 8.09 (d, J=9.0 Hz, 1H), 8.08 (s, 1H), 7.84 (s, 1H), 7.67 (d, J=9.0 Hz, 1H), 7.47 (s, 1H), 7.30 (br s, 5H), 6.43 (br s, 1H), 5.09 (s, 2H), 3.84 (s, 3H), 1.72 (s, 9H). Mass spec.: 452 (MH)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07754732B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-e492e8c9f07f41848dc9b406cea5895b |
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| Source note | uspto-grants-2010_07 |
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