Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ammonia tetrahydrofuran | HCID 21982362 | — |
| Reactant | 4-(6-Methoxy-4-thiazol-2-yl-phthalazin-1-yl)-butyric acid methyl ester | HCID 54370004 | — |
| Product | HCID 18381691 | HCID 18381691 | 73.1% |
Reaction Steps
A suspension of 4-(6-methoxy-4-thiazol-2-yl-phthalazin-1-yl)-butyric acid methyl ester (1.2 g, 3.5 mmoles), prepared as described in example 115, in NH3/THF (10 ml) was added with THF (15 ml), then placed in autoclave at 85° C. After 1 night the mixture was dried, taken up in CH3OH (30 ml) and saturated with NH3 at 0° C., then heated at 85° C. for 44 hours. The mixture was cooled and dried to give a residue which was chromatographed (eluent: CH2Cl2/CH3OH 95:5 to 90:10). The solid was triturated in CH2Cl2 to give 840 mg of the title compound (yield: 73.1%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06492360B1 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-1c4d183705aa44439aa78905d07ac0f1 |
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| Source note | uspto-grants-2002_12 |
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