HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1162218Generated: October 28, 2026
Pyrrolidine → 5-[(1R)-1-methyl-2-oxo-2-pyrrolidin-1-ylethoxy]-N-[1-(pyridin-2-ylmethyl)-1H-indazol-5-yl]quinazolin-4-amine
https://huagongshe.com/reaction/1162218
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | methyl (2R)-2-[(4-{[1-(pyridin-2-ylmethyl)-1H-indazol-5-yl]amino}quinazolin-5-yl)oxy]propanoate | HCID 86627834 | — |
| Product | 5-[(1R)-1-methyl-2-oxo-2-pyrrolidin-1-ylethoxy]-N-[1-(pyridin-2-ylmethyl)-1H-indazol-5-yl]quinazolin-4-amine | HCID 16117087 | 70% |
Reaction Steps
Using the same procedure as in Example 5, methyl (2R)-2-[(4-{[1-(pyridin-2-ylmethyl)-1H-indazol-5-yl]amino}quinazolin-5-yl)oxy]propanoate (200 mg, 0.44 mmol) was reacted with pyrrolidine (0.22 ml, 2.6 mmol) to give the title compound as a beige solid (152 mg, 70%), except that 3 Å molecular sieve was added and that the crude material was purified on an HPLC column (C18, 5 microns, 19 mm diameter, 100 mm length) of a preparative HPLC-MS system eluting with a mixture of water and acetonitrile containing 2 g/l of ammonium carbonate (gradient). NMR Spectrum 1.60 (d, 3H), 1.81 (m, 2H), 1.94 (m, 2H), 3.47-3.30 (m, 3H), 3.77 (m, 1H), 5.62 (q, 1H), 5.77 (s, 2H), 6.95 (d, 1H), 7.28 (m, 2H), 7.35 (d, 1H), 7.74-7.68 (m, 3H), 7.82 (dd, 1H), 8.15 (s, 1H), 8.53 (m, 3H), 11.07 (br s, 1H); Mass spectrum MH+ 494.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07820683B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-9bd8ec201e46470c8ff5d0b6826f0ef3 |
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| Source note | uspto-grants-2010_10 |
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