HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 575115Generated: October 29, 2026
Ammonia methanol → 4,4-Difluoro-9-(3-hydroxy-3-methyl-but-1-ynyl)-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulene-2-carboxylic acid amide
https://huagongshe.com/reaction/575115
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia methanol | HCID 21705897 | — |
| Reactant | 4,4-Difluoro-9-(3-hydroxy-3-methyl-but-1-ynyl)-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulene-2-carboxylic acid methyl ester | HCID 86693143 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4,4-Difluoro-9-(3-hydroxy-3-methyl-but-1-ynyl)-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulene-2-carboxylic acid amide | HCID 71714731 | 30% |
Reaction Steps
To a solution of 4,4-Difluoro-9-(3-hydroxy-3-methyl-but-1-ynyl)-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulene-2-carboxylic acid methyl ester (86 mg, 0.227 mmol) in THF (5 mL) at room temperature, NH3/CH3OH (self-made, 5 mL) was added. The mixture was stirred at room temperature for 3 h, then concentrated to give a residue which was purified by flash column chromatography (silica gel, EtOAc in hexane from 0 to 50%) to give 4,4-Difluoro-9-(3-hydroxy-3-methyl-but-1-ynyl)-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulene-2-carboxylic acid amide as an off-white solid (25 mg, 30%). 1H NMR (400 MHz, DMSO-d6): δ 8.76 (s, 1H), 8.60 (d, J=2.1 Hz, 1H), 8.18 (s, 1H), 7.46 (dd, J1=8.4 Hz, J2=2.2 Hz, 1H), 7.22 (d, J=8.4 Hz, 1H), 5.49 (s, 1H), 4.75 (t, J=10.7 Hz, 2H), 1.49 (s, 6H); LC-MS (ESI & APCI): 365.4 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09034866B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-fef5ac7ef5e941219f91856f20cf1f58 |
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| Source note | uspto-grants-2015_05 |
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