HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 549026Generated: October 30, 2026
2-Amino-2-methyl-1-propanol → HCID 60055735, compound
https://huagongshe.com/reaction/549026
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Amino-2-methyl-1-propanol | HCID 11807 | — |
| 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 | 2-(5-Methoxy-1-methyl-1H-indol-3-yl)-1H-pyrrolo[2,3-b]pyridine-4-carboxylic acid | HCID 22477204 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 60055735 | HCID 60055735 | — |
Reaction Steps
A solution of 2-(5-methoxy-1-methyl-1H-indol-3-yl)-1H-pyrrolo[2,3-b]pyridine-4 carboxylic acid [32 mg, Example 41(a)] in dry dimethylformamide (10 mL), under nitrogen, was treated with diisopropylethylamine (35 μL) followed by O-(7-azabenzotriazol-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate (38 mg). After stirring at room temperature for 1 hour this mixture was treated with a solution of 2-amino-2-methyl-1-propanol (10.5 μL) in dry dimethylformamide (1 mL) and stirring was then continued for a further 2 hours. The reaction mixture was evaporated and the residue was treated with saturated aqueous sodium bicarbonate solution (15 mL). This mixture was stirred for 1 hour and the resulting yellow solid was filtered, then washed well with water and then dried at 100° C. under vacuum to give the title compound (34 mg) as a yellow solid, m.p. 210-212° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07943616B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-d4cdf6acd04547ba8e8ec03bc01aa718 |
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| Source note | uspto-grants-2011_05 |
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