HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1676702Generated: October 26, 2026
Sodium Hydroxide → 4-(9-cyclopentyl-7,7-difluoro-5-methyl-6-oxo-6,7,8,9-tetrahydro-5H-pyrimido[4,5-b][1,4]diazepin-2-ylamino)-2-fluoro-5-methoxybenzoic acid
https://huagongshe.com/reaction/1676702
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl 4-((9-cyclopentyl-7,7-difluoro-5-methyl-6-oxo-6,7,8,9-tetrahydro-5H-pyrimido[4,5-B][1,4]diazepin-2-YL)amino)-2-fluoro-5-methoxybenzoate | HCID 58015164 | — |
| Solvent | Tetrahydrofurfuryl alcohol | HCID 7360 | — |
| Product | 4-(9-cyclopentyl-7,7-difluoro-5-methyl-6-oxo-6,7,8,9-tetrahydro-5H-pyrimido[4,5-b][1,4]diazepin-2-ylamino)-2-fluoro-5-methoxybenzoic acid | HCID 25253679 | 101.3% |
Reaction Steps
An aqueous solution of 5 mL of aqueous 2M (0.010 mole) of sodium hydroxide was added to a solution of 0.51 g (0.00106 mole) of 4-(9-cyclopentyl-7,7-difluoro-5-methyl-6-oxo-6,7,8,9-tetrahydro-5H-pyrimido[4,5-b][1,4]diazepin-2-yl amino)-2-fluoro-5-methoxy-benzoic acid methyl ester (I-168) in 20 mL of tetrahydrofuran-methanol (3:1). The mixture was heated at 50° C. for 18 hours and then concentrated under reduced pressure. The residue was dissolved in water and acidified to pH 2 with 2M hydrochloric acid. After stirring for 30 minutes, the solid was collected by filtration, washed with water and dried to give 0.50 g of 4-(9-cyclopentyl-7,7-difluoro-5-methyl-6-oxo-6,7,8,9-tetrahydro-5H-pyrimido[4,5-b][1,4]diazepin-2-ylamino)-2-fluoro-5-methoxy-benzoic acid (I-169).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08003785B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-d26453e9109048ac9f5dea4c29c5798d |
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| Source note | uspto-grants-2011_08 |
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