HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256367Generated: October 29, 2026
Trifluoroacetic acid → HCID 67064312, compound
https://huagongshe.com/reaction/1256367
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 67064824 | HCID 67064824 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67064312 | HCID 67064312 | — |
Reaction Steps
tert-Butyl 7-(5-(4-(2-hydroxypropan-2-yl)benzamido)pyrazolo[1,5-a]pyrimidin-7-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate from Step A was dissolved in CH2Cl2 (2 ml). Trifluoroacetic acid (1 ml) was then added at 0° C. The mixture was stirred for 30 minutes at that temperature before being concentrated in vacuo. Residual trifluoroacetic acid was removed azeotropically with toluene twice. The residue was then dissolved in acetonitrile before being purified by preparatory HPLC (20-35% MeCN/H2O gradient+0.01% TFA) to give the titled compound as a white powder. 1H NMR (400 MHz, DMSO-d6) δ=11.22 (s, 1 H), 9.11 (br. s., 2 H), 8.01 (d, J=8.6 Hz, 2 H), 7.99-7.89 (m, 3 H), 7.62 (d, J=8.6 Hz, 2 H), 7.49 (d, J=8.1 Hz, 1 H), 6.40 (s, 1 H), 4.43 (br. s., 2 H), 3.47 (d, J=7.3 Hz, 2 H), 3.16-3.07 (m, 2 H), 2.40 (s, 3 H), 1.46 (s, 6 H); ESI-MS: m/z 442.2 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08461163B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-e60167cb471d492191922ebd0fc1a341 |
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| Source note | uspto-grants-2013_06 |
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