HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 540291Generated: October 29, 2026
[3-(Aminomethyl)oxetan-3-yl]methanamine → HCID 86691433, compound
https://huagongshe.com/reaction/540291
Participants
| Role | Name | HCID | Charge |
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| Reactant | [3-(Aminomethyl)oxetan-3-yl]methanamine | HCID 10953471 | — |
| Reactant | HCID 71255321 | HCID 71255321 | — |
| Product | HCID 86691433 | HCID 86691433 | — |
Reaction Steps
A mixture of 4-(benzyloxy)-2-(1-oxido-2,3-dihydro-1,4-benzothiazepin-4 (5H)-yl)quinazoline-6-carboxylic acid (170 mg, 0.37 mmol) and oxetane-3,3-diyldimethanamine (128 mg, 1.11 mmol) was heated at 170° C. for 30 minutes. Then the reaction mixture was cooled to room temperature and purified by preparative HPLC to afford 4-({[3-(Aminomethyl)oxetan-3-yl]methyl}amino)-2-(1-oxido-2,3-dihydro-1,4-benzothiazepin-4(5H)-yl)quinazoline-6-carboxylic acid, MS obsd. (ESI+) [(M+H)+] 468, 1H NMR (400 MHz, DMSO-d6) δ ppm 8.91-8.61 (m, 2 H), 8.09-8.00 (m, 1 H), 7.77-7.74 (m, 1 H), 7.68-7.65 (m, 1 H), 7.51-7.42 (m, 2 H), 7.27-7.13 (m, 1 H), 5.26-5.17 (m, 2 H), 4.89-4.68 (m, 4 H), 452-4.45 (m, 2 H), 4.40-4.31 (m, 2 H), 4.10-3.84 (m, 2 H), 3.20-3.01 (m, 2 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08871756B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-223e1ba1aca24d3a85e91a0f443e2214 |
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| Source note | uspto-grants-2014_10 |
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