HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432985Generated: November 1, 2026
HCID 86760981, compound → HCID 57029141, compound
https://huagongshe.com/reaction/1432985
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 86760981 | HCID 86760981 | — |
| Reactant | HCID 86760982 | HCID 86760982 | — |
| Product | HCID 57029141 | HCID 57029141 | — |
Reaction Steps
The major epimer is assigned as (3S, 5S)-1-(4-Amino-quinazolin-7-ylmethyl)-4-[3-(5-chloro-thiophen-2-yl)-allyl]-3,5-dimethyl-piperazin-2-one trifluoroacetic acid salt (30.8 mg) and is isolated as a yellow solid with a melting point of 69-72° C. C22H24ClN5OS MS m/z: 442, 444. The minor epimer is assigned as (3S, 5R)-1-(4-Amino-quinazolin-7-ylmethyl)-4-[3-(5-chloro-thiophen-2-yl)-allyl]-3,5-dimethyl-piperazin-2-one trifluoroacetic acid salt (13.1 mg) with a melting point of 67-70° C. C22H24ClN5OS MS m/z: 442, 444. 1H NMR (CD3OD) δ: 8.67 (s, 1H); 8.31 (d, 1H, J=8.56 Hz); 7.83 (s, 1H); 7.74 (d, 2H, J=8.56 Hz); 7.14 (d, 1H, J=15.6 Hz); 6.92 (d, 1H, J=3.74 Hz); 6.10-6.03 (m, 1H); 5.0-4.74 (m, 2H); 4.25-3.63 (m, 6H); 1.78 (d, 3H, J=7.03 Hz); 1.50 (d, 3H, J=6.47 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07612075B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-306e1e4b8825493fb8468cfda54836ed |
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| Source note | uspto-grants-2009_11 |
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